Canonical Allele Identifier: PA916063706
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 435162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Arg959Trp
CA7723566
NM_018193.3:c.2875C>T