Canonical Allele Identifier: PA2826924102
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1415069
ClinVar RCV Id: RCV001945456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Ala56Val
CA360802509
NM_001308122.2:c.167C>T