Canonical Allele Identifier: PA916063448
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 221078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Glu96Lys
CA349390
NM_018193.3:c.286G>A