Canonical Allele Identifier: PA645405070
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Ile404Thr
CA7722946
NM_001113378.1:c.1211T>C