Canonical Allele Identifier: PA2827039276
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 414648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001306913.1:p.His377Arg
CA2249505
NM_001319984.1:c.1130A>G