Canonical Allele Identifier: PA645460595
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 437563
ClinVar RCV Id: RCV000502936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036292.2:p.Thr117Met
CA3933705
NM_012160.5:c.350C>T