Allele Registry

Canonical Allele Identifier: PA916020859

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV001001461

RCV001557968

RCV003942768

ClinVar Variation:

460401

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Val551Leu	CA3404201 NM_001308122.2:c.1651G>C