Most severe consequence
12
missense variant
Alleles
A/G
Location
Chromosome 2:205681 (forward strand)|VCF:2 205681 rs5417869278 A G
HGVS names
This variant has 3 HGVS names - Show
External Links
Original source
EVA2024_rsID_mapped
About this variant
This variant overlaps 3 transcripts.
