Allele Registry

Canonical Allele Identifier: PA108169

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000535447

RCV001546222

RCV002226469

ClinVar Variation:

460398

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Arg471Cys	CA3404150 NM_003060.4:c.1411C>T