Canonical Allele Identifier: PA2580505486
Gene: WWOX HGNC NCBI
ClinVar RCV:
RCV003029012
ClinVar Variation:
2103892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Thr49Ser
CA396842063
NM_130791.4:c.145A>T
CA396842065
NM_130791.4:c.146C>G