Canonical Allele Identifier: PA645404770
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 408254
ClinVar RCV Id: RCV000470517 RCV001115869 RCV003151064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106849.1:p.Gly53Ala
CA7722518
NM_001113378.1:c.158G>C