Canonical Allele Identifier: PA266821
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 93542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077431.1:p.Arg578His
CA266820
NM_001083962.2:c.1733G>A