Allele Registry

Canonical Allele Identifier: PA2828542201

Gene: DST HGNC NCBI

ClinVar RCV:

RCV000603185

RCV001510448

RCV001662662

RCV001692226

RCV001701394

ClinVar Variation:

518376

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361658.1:p.Met5225Ile	CA3867697 NM_001374729.1:c.15675G>A CA364513898 NM_001374729.1:c.15675G>T CA364513899 NM_001374729.1:c.15675G>C