Allele Registry

Canonical Allele Identifier: PA2828542118

Gene: DST HGNC NCBI

ClinVar RCV:

RCV004018424

ClinVar Variation:

3076107

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361658.1:p.Asn5019Lys	CA364516422 NM_001374729.1:c.15057T>G CA364516423 NM_001374729.1:c.15057T>A