Canonical Allele Identifier: PA2826319762
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230156.1:p.Arg556Trp
CA254160
NM_001243227.2:c.1666C>T