Canonical Allele Identifier: PA645404913
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 317261
ClinVar RCV Id: RCV000268016 RCV000763985 RCV003930368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Cys156Tyr
CA7722634
NM_001113378.1:c.467G>A