Canonical Allele Identifier: PA2825565672
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 1396190
ClinVar RCV Id: RCV001891585
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Ile1289_Lys1290del
CA2573151239
NM_001113378.1:c.3864_3869del