Canonical Allele Identifier: PA2826924209
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1482825
ClinVar RCV Id: RCV001995822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Asp122Glu
CA360802910
NM_001308122.2:c.366C>A
CA360802911
NM_001308122.2:c.366C>G