Allele Registry

Canonical Allele Identifier: PA2827491664

Gene: CNTN4 HGNC NCBI

ClinVar RCV:

RCV004299190

ClinVar Variation:

2529789

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337024.1:p.Lys776Glu	CA2227682 NM_001350095.2:c.2326A>G