Canonical Allele Identifier: PA645460858
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437819
ClinVar RCV Id: RCV000500088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036292.2:p.Asp599Gly
CA3933337
NM_012160.5:c.1796A>G