Canonical Allele Identifier: PA658667275
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 460394
ClinVar RCV Id: RCV000545444 RCV002226468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Val413Gly
CA360807808
NM_003060.4:c.1238T>G