Canonical Allele Identifier: PA2827432782
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335145.1:p.Arg420Trp
CA254160
NM_001348216.2:c.1258C>T