Canonical Allele Identifier: PA2825329972
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 241740
ClinVar RCV Id: RCV000232279 RCV000238670 RCV002274950 RCV003967666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018125.1:p.Ala329Gly
CA2249427
NM_001018115.2:c.986C>G