Canonical Allele Identifier: PA2826916268
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2699156
ClinVar RCV Id: RCV003507653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293136.1:p.Leu551Pro
CA402528906
NM_001306207.1:c.1652T>C