Canonical Allele Identifier: PA2828352368
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 207529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356513.1:p.Ser78Asn
CA319094
NM_001369584.1:c.233G>A