Canonical Allele Identifier: PA2830057581
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 1396751
ClinVar RCV Id: RCV001887488
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110420.3:p.Gly166Glu
CA361655172
NM_030793.5:c.497G>A