Canonical Allele Identifier: PA2580372773
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1901598
ClinVar RCV Id: RCV002577093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036292.2:p.Thr99Asn
CA16021230
NM_012160.5:c.296C>A