Canonical Allele Identifier: PA2828688487
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 221078
ClinVar RCV Id: RCV000205204 RCV001115870 RCV001804945 RCV003401110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363840.1:p.Glu96Lys
CA349390
NM_001376911.1:c.286G>A