Canonical Allele Identifier: PA2826322508
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230163.1:p.Arg420Trp
CA254160
NM_001243234.2:c.1258C>T