Canonical Allele Identifier: PA658800270
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 526323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Gln1245Lys
CA8251008
NM_000135.4:c.3733C>A