Allele Registry

Canonical Allele Identifier: PA319092

Gene: TCF4 HGNC NCBI

ClinVar RCV:

RCV000189715

RCV001312621

ClinVar Variation:

207527

HGVS (amino-acid)	Matching Registered Transcripts
NP_001077431.1:p.Ala664Thr	CA319091 NM_001083962.2:c.1990G>A