Canonical Allele Identifier: PA2825055015
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 3092783
ClinVar RCV Id: RCV004383700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Gly1390Ser
CA8250702
NM_000135.4:c.4168G>A