Canonical Allele Identifier: PA2826032835
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1712344
ClinVar RCV Id: RCV002294599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Gly262Ala
CA341828221
NM_001166496.2:c.785G>C