Canonical Allele Identifier: PA916015110
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg1184Pro
CA8251098
NM_001286167.3:c.3551G>C