Canonical Allele Identifier: PA2826924113
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1707680
ClinVar RCV Id: RCV002286659 RCV003269159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Asn64Ile
CA3403807
NM_001308122.2:c.191A>T