Canonical Allele Identifier: PA2580193569
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1710975
ClinVar RCV Id: RCV002292262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Pro1393Leu
CA397483811
NM_001286167.3:c.4178C>T