Canonical Allele Identifier: PA1139761502
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_149075.2:p.Val1115Ile
CA2250364
NM_033084.6:c.3343G>A