Canonical Allele Identifier: PA2828687603
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238307
ClinVar RCV Id: RCV000515122 RCV001082996 RCV002500767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363839.1:p.Ile311Thr
CA7722946
NM_001376910.1:c.932T>C