Canonical Allele Identifier: PA2829898249
Gene: FANCI HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Arg1225Gln
CA251642
NM_018193.3:c.3674G>A