Canonical Allele Identifier: PA645404167
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ser735Gly
CA10649316
NM_000135.4:c.2203A>G