Canonical Allele Identifier: PA2828796821
Gene: CYLD HGNC NCBI
ClinVar RCV:
RCV000257955
ClinVar Variation:
267245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365675.1:p.Arg700Lys
CA10590082
NM_001378746.1:c.2099G>A