Allele Registry

Canonical Allele Identifier: PA2828353788

Gene: TCF4 HGNC NCBI

ClinVar RCV:

RCV000189715

RCV001312621

ClinVar Variation:

207527

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356515.1:p.Ala641Thr	CA319091 NM_001369586.1:c.1921G>A