Canonical Allele Identifier: PA916063521
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 317269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Ser371Gly
CA7722914
NM_018193.3:c.1111A>G