Canonical Allele Identifier: PA2826032905
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 291853
ClinVar RCV Id: RCV000398332 RCV002522050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Ala449Thr
CA1011257
NM_001166496.2:c.1345G>A