Canonical Allele Identifier: PA2830170112
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 415952
ClinVar RCV Id: RCV000480602 RCV001081708 RCV002244944 RCV002244945 RCV003960093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570607.1:p.Arg156Ser
CA8183226
NM_130791.4:c.468G>T
CA396841607
NM_130791.4:c.468G>C