Allele Registry

Canonical Allele Identifier: PA2828540892

Gene: DST HGNC NCBI

ClinVar RCV:

RCV001239513

RCV002402756

ClinVar Variation:

965145

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361651.1:p.Asn7605Ser	CA364504860 NM_001374722.1:c.22814A>G