Canonical Allele Identifier: PA2828797622
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_001365681.1:p.Glu734Gly
CA214926
NM_001378752.1:c.2201A>G