Canonical Allele Identifier: PA1139739480
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Glu693_Glu696del
CA7723272
NM_018193.3:c.2078_2089del