Canonical Allele Identifier: PA1139749550
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 849697
ClinVar RCV Id: RCV001053713 RCV002481980 RCV002553761 RCV003141985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Pro20Leu
CA284502483
NM_130791.4:c.59C>T