Canonical Allele Identifier: PA916063528
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Ile404Thr
CA7722946
NM_018193.3:c.1211T>C