Canonical Allele Identifier: PA2828346228
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 393171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356500.1:p.Leu605Pro
CA16608769
NM_001369571.1:c.1814T>C