Allele Registry

Canonical Allele Identifier: PA2830416637

Gene: DST HGNC NCBI

ClinVar RCV:

RCV001510452

RCV001664906

RCV001664907

ClinVar Variation:

1164480

HGVS (amino-acid)	Matching Registered Transcripts
NP_899236.1:p.Ala5368Thr	CA3866054 NM_183380.4:c.16102G>A