Canonical Allele Identifier: PA916020854
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 568045
ClinVar RCV Id: RCV000688283 RCV002226482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Ala509Thr
CA3404176
NM_001308122.2:c.1525G>A