Canonical Allele Identifier: PA2573213785
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 1396190
ClinVar RCV Id: RCV001891585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363840.1:p.Ile1289_Lys1290del
CA2573151239
NM_001376911.1:c.3864_3869del