Canonical Allele Identifier: PA2741941510
Gene: CNTNAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2574464
ClinVar RCV Id: RCV003319046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054860.1:p.Ser429Arg
CA168690910
NM_014141.6:c.1287C>G
CA369924875
NM_014141.6:c.1285A>C
CA369924881
NM_014141.6:c.1287C>A