Canonical Allele Identifier: PA2827335489
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317533.1:p.Arg579Trp
CA254160
NM_001330604.3:c.1735C>T