Allele Registry

Canonical Allele Identifier: PA916020758

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000022332

RCV000186137

RCV002226449

ClinVar Variation:

38279

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Ala238Val	CA312942 NM_001308122.2:c.713C>T