Canonical Allele Identifier: PA2830313004
Gene: FBXO39 HGNC NCBI

Linked Data

ClinVar Variation Id: 3093708
ClinVar RCV Id: RCV004388991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694962.1:p.Arg173Ser
CA397760841
NM_153230.3:c.519G>C
CA397760843
NM_153230.3:c.519G>T