Canonical Allele Identifier: PA916063448
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_060663.2:p.Glu96Lys
CA349390
NM_018193.3:c.286G>A