Canonical Allele Identifier: PA2580368791
Gene: CNTNAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2011567
ClinVar RCV Id: RCV002829603
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054860.1:p.Gly408Asp
CA369924746
NM_014141.6:c.1223G>A