Canonical Allele Identifier: PA2580274268
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1707670
ClinVar RCV Id: RCV002286649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Phe92Val
CA360802717
NM_003060.4:c.274T>G