Canonical Allele Identifier: PA2828688351
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 972
ClinVar RCV Id: RCV000001023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363839.1:p.Arg1192Gln
CA251642
NM_001376910.1:c.3575G>A