Canonical Allele Identifier: PA2827039771
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 861648
ClinVar RCV Id: RCV001068215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001306913.1:p.Val1115Ile
CA2250364
NM_001319984.1:c.3343G>A