Canonical Allele Identifier: PA2828476176
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 456351
ClinVar RCV Id: RCV000543810 RCV001292722 RCV001821496 RCV001843527 RCV002275050 RCV003942732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361182.1:p.Cys721Ser
CA2250030
NM_001374253.1:c.2162G>C
CA351735258
NM_001374253.1:c.2161T>A