Canonical Allele Identifier: PA916020800
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 529850
ClinVar RCV Id: RCV000635350 RCV001785686 RCV002226475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Thr361Ile
CA3404040
NM_001308122.2:c.1082C>T