Canonical Allele Identifier: PA645460842
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437798
ClinVar RCV Id: RCV000504325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036292.2:p.Pro574Gln
CA3933359
NM_012160.5:c.1721C>A