Canonical Allele Identifier: PA2826321328
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 207529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230161.1:p.Arg32His
CA319094
NM_001243232.1:c.95G>A