Allele Registry

Canonical Allele Identifier: PA2828796293

Gene: CYLD HGNC NCBI

ClinVar RCV:

RCV000257955

ClinVar Variation:

267245

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365672.1:p.Arg703Lys	CA10590082 NM_001378743.1:c.2108G>A