Canonical Allele Identifier: PA2741904747
Gene: CNTNAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2523955
ClinVar RCV Id: RCV003289896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003623.1:p.Ala434Thr
CA290793164
NM_003632.3:c.1300G>A