Canonical Allele Identifier: PA2826032799
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2300281
ClinVar RCV Id: RCV002878561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Leu194Phe
CA341828664
NM_001166496.2:c.580C>T