Canonical Allele Identifier: PA916014946
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ser735Gly
CA10649316
NM_001286167.3:c.2203A>G