Canonical Allele Identifier: PA2825330244
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 456351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018125.1:p.Cys758Ser
CA2250030
NM_001018115.2:c.2273G>C
CA351735258
NM_001018115.2:c.2272T>A