Canonical Allele Identifier: PA891861565
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 583183
ClinVar RCV Id: RCV000707454 RCV001849430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Ile73Phe
CA7722537
NM_001113378.1:c.217A>T