Canonical Allele Identifier: PA2828688581
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 2416145
ClinVar RCV Id: RCV003106894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363840.1:p.Ser200Ile
CA274538993
NM_001376911.1:c.599G>T