Canonical Allele Identifier: PA2825052894
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 522334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ile525Val
CA8252237
NM_000135.4:c.1573A>G