Canonical Allele Identifier: PA658800273
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 526419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ala1284Thr
CA8250924
NM_000135.4:c.3850G>A