Canonical Allele Identifier: PA2827432097
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2699156
ClinVar RCV Id: RCV003507653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335143.1:p.Leu414Pro
CA402528906
NM_001348214.2:c.1241T>C