Allele Registry

Canonical Allele Identifier: PA2829832742

Gene: DST HGNC NCBI

ClinVar RCV:

RCV001510452

RCV001664906

RCV001664907

ClinVar Variation:

1164480

HGVS (amino-acid)	Matching Registered Transcripts
NP_056363.2:p.Ala5042Thr	CA3866054 NM_015548.5:c.15124G>A