Canonical Allele Identifier: PA2828797131
Gene: CYLD HGNC NCBI

Linked Data

ClinVar Variation Id: 319497
ClinVar RCV Id: RCV000311859 RCV000370163 RCV000404707 RCV002264928 RCV003469254
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365678.1:p.Ile20Ser
CA8052119
NM_001378749.1:c.59T>G