Allele Registry

Canonical Allele Identifier: PA2825865711

Gene: DST HGNC NCBI

ClinVar RCV:

RCV004018424

ClinVar Variation:

3076107

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138241.1:p.Asn3111Lys	CA364516422 NM_001144769.5:c.9333T>G CA364516423 NM_001144769.5:c.9333T>A