Canonical Allele Identifier: PA159442
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134313
ClinVar RCV Id: RCV000120987 RCV000459559 RCV000764454 RCV001004843 RCV001541664 RCV003415914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149075.2:p.Pro593Ser
CA159438
NM_033084.6:c.1777C>T