Canonical Allele Identifier: PA645404030
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg435His
CA16615049
NM_000135.4:c.1304G>A