Allele Registry

Canonical Allele Identifier: PA314101

Gene: CNTNAP2 HGNC NCBI

ClinVar RCV:

RCV000187174

RCV000227817

RCV000515191

RCV002314708

RCV003480545

RCV003955123

ClinVar Variation:

205233

HGVS (amino-acid)	Matching Registered Transcripts
NP_054860.1:p.Ser382Asn	CA314100 NM_014141.6:c.1145G>A