Canonical Allele Identifier: PA2826614028
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437797
ClinVar RCV Id: RCV000502546 RCV001857198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265645.1:p.Met571Ile
CA3933360
NM_001278716.2:c.1713G>A
CA365085073
NM_001278716.2:c.1713G>T
CA365085078
NM_001278716.2:c.1713G>C