Canonical Allele Identifier: PA2826916337
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 207529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293137.1:p.Arg32His
CA319094
NM_001306208.1:c.95G>A