Allele Registry

Canonical Allele Identifier: PA645431006

Gene: CNTNAP2 HGNC NCBI

ClinVar Variation Id: 373502

HGVS (amino-acid)	Matching Registered Transcripts
NP_054860.1:p.Ser443Arg	CA4546021 NM_014141.6:c.1329C>A CA369924971 NM_014141.6:c.1327A>C CA369924976 NM_014141.6:c.1329C>G