Canonical Allele Identifier: PA2826816151
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 373531
ClinVar RCV Id: RCV000414593 RCV000532362 RCV001591051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278926.1:p.Lys171Arg
CA16043024
NM_001291997.2:c.512A>G