Canonical Allele Identifier: PA108289
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1068475
ClinVar RCV Id: RCV001380048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Leu507Ser
CA360809843
NM_003060.4:c.1520T>C