Canonical Allele Identifier: PA645502251
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 285771
ClinVar Variation Id: 2955851
ClinVar RCV Id: RCV003811002

Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_003051.1:p.Gly12Asp