Canonical Allele Identifier: PA314113
Gene: CNTNAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205239
ClinVar RCV Id: RCV000187180 RCV004020266
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054860.1:p.Asp425Asn
CA314112
NM_014141.6:c.1273G>A