Canonical Allele Identifier: PA2828353727
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356515.1:p.Arg557Trp
CA254160
NM_001369586.1:c.1669C>T