Canonical Allele Identifier: PA314103
Gene: CNTNAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205234
ClinVar RCV Id: RCV000187175 RCV000766790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054860.1:p.Asn391Lys
CA314102
NM_014141.6:c.1173C>G
CA369924634
NM_014141.6:c.1173C>A