Allele Registry

Canonical Allele Identifier: PA2828545980

Gene: DST HGNC NCBI

ClinVar RCV:

RCV001510452

RCV001664906

RCV001664907

ClinVar Variation:

1164480

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361663.1:p.Ala7674Thr	CA3866054 NM_001374734.1:c.23020G>A