Canonical Allele Identifier: PA2829865017
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2103892
ClinVar RCV Id: RCV003029012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057457.1:p.Thr49Ser
CA396842063
NM_016373.4:c.145A>T
CA396842065
NM_016373.4:c.146C>G