Canonical Allele Identifier: PA2828351770
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 393171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356511.1:p.Leu581Pro
CA16608769
NM_001369582.1:c.1742T>C