Canonical Allele Identifier: PA2573317552
Gene: FBXO38 HGNC NCBI
ClinVar RCV:
RCV002039130
ClinVar Variation:
1523775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_995308.1:p.Val120Leu
CA361654829
NM_205836.3:c.358G>T
CA361654831
NM_205836.3:c.358G>C