Canonical Allele Identifier: PA256196
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149075.2:p.Arg1236His
CA256193
NM_033084.6:c.3707G>A