Canonical Allele Identifier: PA2580505486
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 2103892
ClinVar RCV Id: RCV003029012

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