Canonical Allele Identifier: PA2828796960
Gene: CYLD HGNC NCBI

Linked Data

ClinVar Variation Id: 5258
ClinVar RCV Id: RCV000005571 RCV000005572
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365676.1:p.Glu744Gly
CA214926
NM_001378747.1:c.2231A>G