Canonical Allele Identifier: PA2826032830
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2104664
ClinVar RCV Id: RCV003014740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Gln251Glu
CA341828297
NM_001166496.2:c.751C>G