Canonical Allele Identifier: PA2826032815
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2002363
ClinVar RCV Id: RCV002820352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Asp225Val
CA1011390
NM_001166496.2:c.674A>T