Canonical Allele Identifier: PA916063589
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 456195
ClinVar RCV Id: RCV000537549 RCV002490946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Ala579Thr
CA7723137
NM_018193.3:c.1735G>A