Canonical Allele Identifier: PA159292
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg894Lys
CA159290
NM_000135.4:c.2681G>A