Canonical Allele Identifier: PA2828687739
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 456195
ClinVar RCV Id: RCV000537549 RCV002490946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363839.1:p.Ala486Thr
CA7723137
NM_001376910.1:c.1456G>A