Canonical Allele Identifier: PA916063609
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 456197
ClinVar RCV Id: RCV000527436 RCV001770406 RCV002476094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Met604Val
CA7723159
NM_018193.3:c.1810A>G