Canonical Allele Identifier: PA2828688472
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_001363840.1:p.Gly79Glu
CA393738000
NM_001376911.1:c.236G>A