Canonical Allele Identifier: PA2828688665
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363840.1:p.Asn302Ser
CA7722832
NM_001376911.1:c.905A>G