Allele Registry

Canonical Allele Identifier: PA2829831862

Gene: DST HGNC NCBI

ClinVar RCV:

RCV000603185

RCV001510448

RCV001662662

RCV001692226

RCV001701394

ClinVar Variation:

518376

HGVS (amino-acid)	Matching Registered Transcripts
NP_056363.2:p.Met2813Ile	CA3867697 NM_015548.5:c.8439G>A CA364513898 NM_015548.5:c.8439G>T CA364513899 NM_015548.5:c.8439G>C