Canonical Allele Identifier: PA645406768
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 241738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149075.2:p.Ile104Thr
CA2249178
NM_033084.6:c.311T>C