Allele Registry

Canonical Allele Identifier: PA2826291044

Gene: CNTN4 HGNC NCBI

ClinVar RCV:

RCV004299190

ClinVar Variation:

2529789

HGVS (amino-acid)	Matching Registered Transcripts
NP_001193884.1:p.Lys776Glu	CA2227682 NM_001206955.2:c.2326A>G