Canonical Allele Identifier: PA2828476827
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12038
ClinVar RCV Id: RCV000012818 RCV001265744 RCV002512995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361182.1:p.Arg1199His
CA256193
NM_001374253.1:c.3596G>A