Canonical Allele Identifier: PA2825055001
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1043138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg1382Thr
CA8250774
NM_000135.4:c.4145G>C