Canonical Allele Identifier: PA2826322532
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 393171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230163.1:p.Leu449Pro
CA16608769
NM_001243234.2:c.1346T>C