Allele Registry

Canonical Allele Identifier: PA1139743818

Gene: DST HGNC NCBI

ClinVar RCV:

RCV001239513

RCV002402756

ClinVar Variation:

965145

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361665.1:p.Asn7629Ser	CA364504860 NM_001374736.1:c.22886A>G