Canonical Allele Identifier: PA2827039802
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 526384
ClinVar RCV Id: RCV000630908 RCV002528847 RCV003153771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001306913.1:p.Arg1165Gln
CA2250423
NM_001319984.1:c.3494G>A