Canonical Allele Identifier: PA645460798
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437751
ClinVar RCV Id: RCV000499656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036292.2:p.Ile464Val
CA3933447
NM_012160.5:c.1390A>G