Canonical Allele Identifier: PA2826032814
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2005104
ClinVar RCV Id: RCV002820772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Asp225Tyr
CA341828465
NM_001166496.2:c.673G>T