Canonical Allele Identifier: PA1139749599
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 854717
ClinVar RCV Id: RCV001059820 RCV002553872 RCV001760018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Lys28Gln
CA8182987
NM_130791.4:c.82A>C