Canonical Allele Identifier: PA916020838
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 25420
ClinVar RCV Id: RCV000022376 RCV000080049 RCV002251921 RCV002281715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Tyr473Asp
CA285513
NM_001308122.2:c.1417T>G