Canonical Allele Identifier: PA159321
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg1195Gln
CA159319
NM_000135.4:c.3584G>A