Canonical Allele Identifier: PA2828687729
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 526471
ClinVar RCV Id: RCV000631005 RCV001115981 RCV003980218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363839.1:p.His475Arg
CA7723130
NM_001376910.1:c.1424A>G