Canonical Allele Identifier: PA645403909
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Asp229Asn
CA8252858
NM_000135.4:c.685G>A