Canonical Allele Identifier: PA2825400710
Gene: CYLD HGNC NCBI

Linked Data

ClinVar Variation Id: 5258

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035877.1:p.Glu744Gly
CA214926
NM_001042412.3:c.2231A>G