Canonical Allele Identifier: PA2742036717
Gene: FBXO38 HGNC NCBI
ClinVar RCV:
RCV003597033
ClinVar Variation:
2756418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_995308.1:p.Glu83Lys
CA361654305
NM_205836.3:c.247G>A