Canonical Allele Identifier: PA1139716481
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 917533
ClinVar RCV Id: RCV001174538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036292.2:p.Gly513Val
CA365087128
NM_012160.5:c.1538G>T