Canonical Allele Identifier: PA2573088727
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338895
ClinVar RCV Id: RCV001823349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Ala143Val
CA413656486
NM_006517.5:c.428C>T