Canonical Allele Identifier: PA2828796299
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_001365672.1:p.Glu747Gly
CA214926
NM_001378743.1:c.2240A>G