Canonical Allele Identifier: PA1139686696
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 550150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Leu1320del
CA286617244
NM_001286167.3:c.3959_3961del