Canonical Allele Identifier: PA891848767
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 568045
ClinVar RCV Id: RCV000688283 RCV002226482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Ala485Thr
CA3404176
NM_003060.4:c.1453G>A