Canonical Allele Identifier: PA2825564708
Gene: FANCI HGNC NCBI
ClinVar RCV:
RCV003637544
ClinVar Variation:
2917627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Gln3His
CA393736284
NM_001113378.1:c.9G>C
CA393736285
NM_001113378.1:c.9G>T