Canonical Allele Identifier: PA2828478828
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 456359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361183.1:p.Thr1338Met
CA2250621
NM_001374254.1:c.4013C>T