Canonical Allele Identifier: PA2828688351
Gene: FANCI HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363839.1:p.Arg1192Gln
CA251642
NM_001376910.1:c.3575G>A