Allele Registry

Canonical Allele Identifier: PA916020862

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000316258

RCV001859650

ClinVar Variation:

286533

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Met565Leu	CA3404222 NM_001308122.2:c.1693A>T CA360810241 NM_001308122.2:c.1693A>C