Canonical Allele Identifier: PA2828687961
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 408253
ClinVar RCV Id: RCV000463193 RCV001821273 RCV001121010 RCV003237865 RCV004022682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363839.1:p.Asn743Ser
CA16614575
NM_001376910.1:c.2228A>G