Allele Registry

Canonical Allele Identifier: PA2825867785

Gene: DST HGNC NCBI

ClinVar RCV:

RCV004018424

ClinVar Variation:

3076107

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138242.1:p.Asn2973Lys	CA364516422 NM_001144770.2:c.8919T>G CA364516423 NM_001144770.2:c.8919T>A