Allele Registry

Canonical Allele Identifier: PA2830169862

Gene: CNTNAP5 HGNC NCBI

ClinVar RCV:

RCV003979127

ClinVar Variation:

3056463

HGVS (amino-acid)	Matching Registered Transcripts
NP_570129.1:p.Ser452Leu	CA1855846 NM_130773.4:c.1355C>T