Allele Registry

Canonical Allele Identifier: PA108080

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000006797

RCV000186157

ClinVar Variation:

6428

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Ala442Ile	CA312974 NM_003060.4:c.1324_1325delinsAT