Allele Registry

Canonical Allele Identifier: PA2828796299

Gene: CYLD HGNC NCBI

ClinVar RCV:

RCV000005571

RCV000005572

ClinVar Variation:

5258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365672.1:p.Glu747Gly	CA214926 NM_001378743.1:c.2240A>G