Canonical Allele Identifier: PA314095
Gene: CNTNAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205230
ClinVar RCV Id: RCV000187171 RCV000232850 RCV003343678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054860.1:p.Asn360Asp
CA314094
NM_014141.6:c.1078A>G