Canonical Allele Identifier: PA1139737115
Gene: CNTNAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 937631
ClinVar RCV Id: RCV001206685 RCV002379783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054860.1:p.Gly344Asp
CA369924327
NM_014141.6:c.1031G>A