Canonical Allele Identifier: PA2826587455
Gene: FBXL7 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265246.1:p.Arg322His
CA3209611
NM_001278317.2:c.965G>A