Allele Registry

Canonical Allele Identifier: PA2828796171

Gene: CYLD HGNC NCBI

ClinVar Allele:

341665

ClinVar RCV:

RCV000311859

RCV000370163

RCV000404707

RCV002264928

RCV003469254

ClinVar Variation:

319497

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365672.1:p.Ile20Ser	CA8052119 NM_001378743.1:c.59T>G