Canonical Allele Identifier: PA2829898251
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 1396190
ClinVar RCV Id: RCV001891585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Ile1229_Lys1230del
CA2573151239
NM_018193.3:c.3684_3689del