Canonical Allele Identifier: PA2826537738
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 1780978
ClinVar RCV Id: RCV004059427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258652.1:p.Glu611Gly
CA361655594
NM_001271723.2:c.1832A>G