Canonical Allele Identifier: PA097515
Gene: CYLD HGNC NCBI

Linked Data

ClinVar Variation Id: 5258

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056062.1:p.Glu747Gly
CA214926
NM_015247.3:c.2240A>G