Canonical Allele Identifier: PA645405204
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Glu693_Glu696del
CA7723272
NM_001113378.1:c.2078_2089del