Canonical Allele Identifier: PA2828476620
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 861648
ClinVar RCV Id: RCV001068215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361182.1:p.Val1078Ile
CA2250364
NM_001374253.1:c.3232G>A