Allele Registry

Canonical Allele Identifier: PA2827335788

Gene: TCF4 HGNC NCBI

ClinVar Variation Id: 574403

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317534.1:p.Gly298Val	CA300814398 NM_001330605.3:c.893G>T