Canonical Allele Identifier: PA645405112
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238309
ClinVar RCV Id: RCV000228956 RCV000482252 RCV000766508 RCV001094276 RCV003955318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Met525Val
CA7723058
NM_001113378.1:c.1573A>G