Canonical Allele Identifier: PA2828350741
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2699156
ClinVar RCV Id: RCV003507653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356509.1:p.Leu554Pro
CA402528906
NM_001369580.1:c.1661T>C