Canonical Allele Identifier: PA645497229
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 241106
ClinVar RCV Id: RCV000443525 RCV001080349 RCV001820753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Leu272Phe
CA8183503
NM_016373.4:c.816G>T
CA396843077
NM_016373.4:c.816G>C