Canonical Allele Identifier: PA645460832
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437785
ClinVar RCV Id: RCV000500747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036292.2:p.Cys558Gly
CA3933407
NM_012160.5:c.1672T>G