Canonical Allele Identifier: PA2828351748
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356511.1:p.Arg552Trp
CA254160
NM_001369582.1:c.1654C>T