Canonical Allele Identifier: PA234951
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 167696
ClinVar RCV Id: RCV000153959 RCV000411999 RCV002226458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Cys113Tyr
CA234950
NM_003060.4:c.338G>A