Canonical Allele Identifier: PA916020827
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_001295051.1:p.Val437Gly
CA360807808
NM_001308122.2:c.1310T>G