Canonical Allele Identifier: PA916020814
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 460391
ClinVar RCV Id: RCV000552913 RCV001509256 RCV001274337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Met405Thr
CA3404091
NM_001308122.2:c.1214T>C