Canonical Allele Identifier: PA2826537504
Gene: FBXO38 HGNC NCBI
ClinVar RCV:
RCV001887488
ClinVar Variation:
1396751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258652.1:p.Gly166Glu
CA361655172
NM_001271723.2:c.497G>A