Allele Registry

Canonical Allele Identifier: PA2830380948

Gene: CNTN4 HGNC NCBI

ClinVar RCV:

RCV004299190

ClinVar Variation:

2529789

HGVS (amino-acid)	Matching Registered Transcripts
NP_783302.1:p.Lys448Glu	CA2227682 NM_175613.3:c.1342A>G