Canonical Allele Identifier: PA2827431723
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335142.1:p.Arg450Trp
CA254160
NM_001348213.2:c.1348C>T