Canonical Allele Identifier: PA1139749546
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 968820
ClinVar RCV Id: RCV001244041 RCV003284115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Asp10His
CA8182978
NM_130791.4:c.28G>C