Allele Registry

Canonical Allele Identifier: PA2828797362

Gene: CYLD HGNC NCBI

ClinVar RCV:

RCV000005571

RCV000005572

ClinVar Variation:

5258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365679.1:p.Glu744Gly	CA214926 NM_001378750.1:c.2231A>G