Canonical Allele Identifier: PA2828688402
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 2917627
ClinVar RCV Id: RCV003637544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363840.1:p.Gln3His
CA393736284
NM_001376911.1:c.9G>C
CA393736285
NM_001376911.1:c.9G>T