Canonical Allele Identifier: PA2828347729
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2699156
ClinVar RCV Id: RCV003507653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356503.1:p.Leu574Pro
CA402528906
NM_001369574.1:c.1721T>C