Allele Registry

Canonical Allele Identifier: PA2826291119

Gene: CNTN4 HGNC NCBI

ClinVar RCV:

RCV004299190

ClinVar Variation:

2529789

HGVS (amino-acid)	Matching Registered Transcripts
NP_001193885.1:p.Lys447Glu	CA2227682 NM_001206956.2:c.1339A>G