Canonical Allele Identifier: PA891848643
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 575689
ClinVar RCV Id: RCV000697982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Val40Glu
CA360802415
NM_003060.4:c.119T>A