Canonical Allele Identifier: PA2830057854
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 1780978
ClinVar RCV Id: RCV004059427
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110420.3:p.Glu611Gly
CA361655594
NM_030793.5:c.1832A>G