Canonical Allele Identifier: PA2827039843
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_001306913.1:p.Arg1236His
CA256193
NM_001319984.1:c.3707G>A