Canonical Allele Identifier: PA2580293895
Gene: CNTNAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2440174
ClinVar RCV Id: RCV003145074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003623.1:p.Tyr23His
CA399632018
NM_003632.3:c.67T>C