Canonical Allele Identifier: PA2826323270
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230165.1:p.Arg416Trp
CA254160
NM_001243236.2:c.1246C>T