Canonical Allele Identifier: PA916063674
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 408251
ClinVar RCV Id: RCV000471427 RCV002481431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Ile735Thr
CA16614749
NM_018193.3:c.2204T>C