Canonical Allele Identifier: PA2828687572
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_001363839.1:p.Ser278Gly
CA7722914
NM_001376910.1:c.832A>G