Allele Registry

Canonical Allele Identifier: PA2830416597

Gene: DST HGNC NCBI

ClinVar RCV:

RCV001239513

RCV002402756

ClinVar Variation:

965145

HGVS (amino-acid)	Matching Registered Transcripts
NP_899236.1:p.Asn5308Ser	CA364504860 NM_183380.4:c.15923A>G