Canonical Allele Identifier: PA2828349236
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356506.1:p.Arg555Trp
CA254160
NM_001369577.1:c.1663C>T