Canonical Allele Identifier: PA2573254789
Gene: CNTNAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1345965
ClinVar RCV Id: RCV002029763
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054860.1:p.Gly408Ser
CA369924744
NM_014141.6:c.1222G>A