Canonical Allele Identifier: PA2573229343
Gene: CNTNAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1679401
ClinVar RCV Id: RCV002226998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003623.1:p.Gly349Val
CA399637522
NM_003632.3:c.1046G>T