Canonical Allele Identifier: PA645460854
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437485
ClinVar RCV Id: RCV000500771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036292.2:p.Asp591Gly
CA16021023
NM_012160.5:c.1772A>G