Canonical Allele Identifier: PA658661316
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg1321His
CA8250848
NM_000135.4:c.3962G>A