Canonical Allele Identifier: PA2826924019
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1065994
ClinVar RCV Id: RCV001376870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Gly15Glu
CA3403772
NM_001308122.2:c.44G>A