Canonical Allele Identifier: PA658660931
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 456344
ClinVar RCV Id: RCV000552393 RCV001092962 RCV000764453 RCV003488659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149075.2:p.Ile450Val
CA2249616
NM_033084.6:c.1348A>G