Canonical Allele Identifier: PA2828688721
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 317269
ClinVar RCV Id: RCV000294568 RCV001094369 RCV003920334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363840.1:p.Ser371Gly
CA7722914
NM_001376911.1:c.1111A>G