Canonical Allele Identifier: PA2827039898
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 456358
ClinVar RCV Id: RCV000535262 RCV002506293 RCV003153680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001306913.1:p.Leu1325Met
CA2250597
NM_001319984.1:c.3973C>A