Canonical Allele Identifier: PA916020773
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 529846
ClinVar RCV Id: RCV000635346 RCV002226473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Thr288Met
CA3403969
NM_001308122.2:c.863C>T