Canonical Allele Identifier: PA2573317601
Gene: FBXO38 HGNC NCBI

Linked Data

ClinVar Variation Id: 1466018
ClinVar RCV Id: RCV001979507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_995308.1:p.Asp601Tyr
CA361655489
NM_205836.3:c.1801G>T