Canonical Allele Identifier: PA2828479018
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 456361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361184.1:p.Gln26His
CA2249106
NM_001374255.1:c.78A>C
CA351717922
NM_001374255.1:c.78A>T