Canonical Allele Identifier: PA645431000
Gene: CNTNAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 420402
ClinVar RCV Id: RCV000481495 RCV001370377
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054860.1:p.Ser443Asn
CA16618377
NM_014141.6:c.1328G>A