Allele Registry

Canonical Allele Identifier: PA1139699896

Gene: CTNND1 HGNC NCBI

ClinVar RCV:

RCV001034561

RCV003389857

ClinVar Variation:

834016

HGVS (amino-acid)	Matching Registered Transcripts
NP_001322.1:p.Leu558Phe	CA6010480 NM_001331.3:c.1672C>T