Canonical Allele Identifier: PA2829723891
Gene: FBXO7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3093805
ClinVar RCV Id: RCV004389088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036311.3:p.Leu7Val
CA10201293
NM_012179.4:c.19C>G