Allele Registry

Canonical Allele Identifier: PA916020739

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000550851

RCV000623583

ClinVar Variation:

460408

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Gly176Asp	CA3403893 NM_001308122.2:c.527G>A