Canonical Allele Identifier: PA2573296798
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1355835
ClinVar RCV Id: RCV001867126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Asn36Ile
CA396841955
NM_130791.4:c.107A>T