Canonical Allele Identifier: PA2826321284
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 393171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230160.1:p.Leu563Pro
CA16608769
NM_001243231.2:c.1688T>C