Allele Registry

Canonical Allele Identifier: PA2828797089

Gene: CYLD HGNC NCBI

ClinVar RCV:

RCV000257955

ClinVar Variation:

267245

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365677.1:p.Arg700Lys	CA10590082 NM_001378748.1:c.2099G>A