Allele Registry

Canonical Allele Identifier: PA658667192

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000550851

RCV000623583

ClinVar Variation:

460408

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Gly152Asp	CA3403893 NM_003060.4:c.455G>A