Canonical Allele Identifier: PA108250
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 25349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Gly12Ser
CA312960
NM_003060.4:c.34G>A