Allele Registry

Canonical Allele Identifier: PA2826924020

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000006798

RCV000186150

ClinVar Variation:

6429

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Gly15Trp	CA312963 NM_001308122.2:c.43G>T