Canonical Allele Identifier: PA2828687490
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 449021
ClinVar RCV Id: RCV000523947 RCV000529696 RCV001118938 RCV001821453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363839.1:p.Ile182Thr
CA7722781
NM_001376910.1:c.545T>C