Canonical Allele Identifier: PA2499282727
Gene: WWOX HGNC NCBI
ClinVar RCV:
RCV001352381
ClinVar Variation:
1047640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Cys362Arg
CA396536991
NM_016373.4:c.1084T>C