Canonical Allele Identifier: PA2826537480
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 1523775
ClinVar RCV Id: RCV002039130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258652.1:p.Val120Leu
CA361654829
NM_001271723.2:c.358G>T
CA361654831
NM_001271723.2:c.358G>C