Canonical Allele Identifier: PA2830057536
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 2756418
ClinVar RCV Id: RCV003597033
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110420.3:p.Glu83Lys
CA361654305
NM_030793.5:c.247G>A