Canonical Allele Identifier: PA2829418998
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 935824
ClinVar RCV Id: RCV001204498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Leu199Pro
CA360804812
NM_003060.4:c.596T>C