Canonical Allele Identifier: PA2828797089
Gene: CYLD HGNC NCBI

Linked Data

ClinVar Variation Id: 267245
ClinVar RCV Id: RCV000257955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365677.1:p.Arg700Lys
CA10590082
NM_001378748.1:c.2099G>A