Canonical Allele Identifier: PA2825329332
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018122.1:p.His292Asp
CA8252711
NM_001018112.2:c.874C>G