Most severe consequence
12
missense variant
Alleles
T/C
Location
Chromosome 4:49973871 (forward strand)|VCF:4 49973871 rs870394693 T C
HGVS names
This variant has 3 HGVS names - Show
External Links
Original source
EVA2024_rsID_mapped
About this variant
This variant overlaps 2 transcripts.
