Canonical Allele Identifier: PA100029
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 100649
ClinVar RCV Id: RCV000087049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Pro47Thr
CA150589
NM_016373.4:c.139C>A