Canonical Allele Identifier: PA2828349741
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356507.1:p.Arg555Trp
CA254160
NM_001369578.1:c.1663C>T