Canonical Allele Identifier: PA916063582
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 526471
ClinVar RCV Id: RCV000631005 RCV001115981 RCV003980218
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.His568Arg
CA7723130
NM_018193.3:c.1703A>G