Canonical Allele Identifier: PA2826032805
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2416661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159968.1:p.Pro202Ser
CA1011401
NM_001166496.2:c.604C>T