Canonical Allele Identifier: PA891861046
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 574403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077431.1:p.Gly428Val
CA300814398
NM_001083962.2:c.1283G>T