Canonical Allele Identifier: PA2826032837
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1968163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Leu267Val
CA341828190
NM_001166496.2:c.799C>G