Canonical Allele Identifier: PA2828688354
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 1396190
ClinVar RCV Id: RCV001891585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363839.1:p.Ile1196_Lys1197del
CA2573151239
NM_001376910.1:c.3585_3590del