Canonical Allele Identifier: PA100009
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 100648
ClinVar RCV Id: RCV000087048 RCV001091765
ClinVar Variation Id: 1390703
ClinVar RCV Id: RCV001891133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Gly372Arg
CA150588
NM_016373.4:c.1114G>C
CA396537069
NM_016373.4:c.1114G>A