Canonical Allele Identifier: PA916058938
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 241098
ClinVar RCV Id: RCV000230460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Tyr34Cys
CA10583429
NM_130791.4:c.101A>G