Canonical Allele Identifier: PA2830057555
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 1523775
ClinVar RCV Id: RCV002039130
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110420.3:p.Val120Leu
CA361654829
NM_030793.5:c.358G>T
CA361654831
NM_030793.5:c.358G>C