Canonical Allele Identifier: PA645405528
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 408231
ClinVar RCV Id: RCV000476737 RCV000765231 RCV002223211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Gly1316Arg
CA7723992
NM_001113378.1:c.3946G>A
CA393746444
NM_001113378.1:c.3946G>C