Canonical Allele Identifier: PA2828797655
Gene: CYLD HGNC NCBI

Linked Data

ClinVar Variation Id: 1319761
ClinVar RCV Id: RCV003238016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365681.1:p.Met939Leu
CA395886392
NM_001378752.1:c.2815A>C
CA395886397
NM_001378752.1:c.2815A>T