Canonical Allele Identifier: PA916063421
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 408254

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Gly53Ala
CA7722518
NM_018193.3:c.158G>C