Canonical Allele Identifier: PA2825054992
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1063615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Pro1378Leu
CA8250776
NM_000135.4:c.4133C>T