Canonical Allele Identifier: PA2826032806
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1965870
ClinVar RCV Id: RCV002745377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Thr203Ala
CA1011400
NM_001166496.2:c.607A>G