Canonical Allele Identifier: PA645460594
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437562
ClinVar RCV Id: RCV000500795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036292.2:p.Leu112Trp
CA3933706
NM_012160.5:c.335T>G