Canonical Allele Identifier: PA2826032809
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2787198
ClinVar RCV Id: RCV003660621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Gly206Arg
CA341828592
NM_001166496.2:c.616G>C
CA341828593
NM_001166496.2:c.616G>A