Canonical Allele Identifier: PA2826714531
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 3092783
ClinVar RCV Id: RCV004383700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Gly1391Glu
CA8250702
NM_001286167.3:c.4172G>A