Canonical Allele Identifier: PA222961
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Gln138Glu
CA222960
NM_006517.5:c.412C>G