Canonical Allele Identifier: PA891848743
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 574461
ClinVar RCV Id: RCV000696397 RCV002226484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Leu419Val
CA3404107
NM_003060.4:c.1255C>G