Allele Registry

Canonical Allele Identifier: PA915966248

Gene: SLC10A2 HGNC NCBI

ClinVar RCV:

RCV000730269

RCV003897574

RCV003984832

ClinVar Variation:

242727

HGVS (amino-acid)	Matching Registered Transcripts
NP_000443.2:p.Thr262Met	CA031677 NM_000452.3:c.785C>T CA031856 NM_000452.3:c.[785C>T;728T>C]