Canonical Allele Identifier: PA2826924079
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 529851
ClinVar RCV Id: RCV000635352 RCV002226476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Thr45Ala
CA3403795
NM_001308122.2:c.133A>G