Allele Registry

Canonical Allele Identifier: PA916020833

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000006797

RCV000186157

ClinVar Variation:

6428

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Ala466Ile	CA312974 NM_001308122.2:c.1396_1397delinsAT