Canonical Allele Identifier: PA2829461514
Gene: CNTNAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3146817
ClinVar RCV Id: RCV004442187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003623.1:p.Ile363Ser
CA399637684
NM_003632.3:c.1088T>G