Canonical Allele Identifier: PA916063613
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 317280
ClinVar RCV Id: RCV000277965 RCV001094314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Leu619Gln
CA7723181
NM_018193.3:c.1856T>A