Canonical Allele Identifier: PA658661527
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 456219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Ile1289Val
CA7723936
NM_001113378.1:c.3865A>G