Canonical Allele Identifier: PA2828688355
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 456219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363839.1:p.Ile1196Val
CA7723936
NM_001376910.1:c.3586A>G