Canonical Allele Identifier: PA2826319382
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 207529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230156.1:p.Ser78Asn
CA319094
NM_001243227.2:c.233G>A