Canonical Allele Identifier: PA2826032808
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1998347
ClinVar RCV Id: RCV002810397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Ala205Thr
CA341828599
NM_001166496.2:c.613G>A