Canonical Allele Identifier: PA645454428
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230155.2:p.Arg682Trp
CA254160
NM_001243226.3:c.2044C>T