Canonical Allele Identifier: PA916063439
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 456207
ClinVar RCV Id: RCV000543012 RCV002483355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Gly79Glu
CA393738000
NM_018193.3:c.236G>A