Canonical Allele Identifier: PA2828688452
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 317258
ClinVar RCV Id: RCV000356939 RCV001344485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363840.1:p.Arg66Cys
CA7722529
NM_001376911.1:c.196C>T