Allele Registry

Canonical Allele Identifier: PA2830415190

Gene: DST HGNC NCBI

ClinVar RCV:

RCV000603185

RCV001510448

RCV001662662

RCV001692226

RCV001701394

ClinVar Variation:

518376

HGVS (amino-acid)	Matching Registered Transcripts
NP_899236.1:p.Met3139Ile	CA3867697 NM_183380.4:c.9417G>A CA364513898 NM_183380.4:c.9417G>T CA364513899 NM_183380.4:c.9417G>C