Canonical Allele Identifier: PA658800206
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 526342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg756Pro
CA8251806
NM_000135.4:c.2267G>C