Canonical Allele Identifier: PA2828345694
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356499.1:p.Arg579Trp
CA254160
NM_001369570.1:c.1735C>T