Canonical Allele Identifier: PA916063508
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238331
ClinVar RCV Id: RCV000228659 RCV002503894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Asn302Ser
CA7722832
NM_018193.3:c.905A>G