Canonical Allele Identifier: PA2826924105
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1707665
ClinVar RCV Id: RCV002286644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Ser59Arg
CA3403805
NM_001308122.2:c.177C>G
CA360802523
NM_001308122.2:c.175A>C
CA360802529
NM_001308122.2:c.177C>A