Canonical Allele Identifier: PA2828797659
Gene: CYLD HGNC NCBI

Linked Data

ClinVar Variation Id: 319497
ClinVar RCV Id: RCV000311859 RCV000370163 RCV000404707 RCV002264928 RCV003469254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365682.1:p.Ile20Ser
CA8052119
NM_001378753.1:c.59T>G