Canonical Allele Identifier: PA2826032811
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1441149
ClinVar RCV Id: RCV001950569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Asp208Glu
CA29390960
NM_001166496.2:c.624T>A
CA341828575
NM_001166496.2:c.624T>G