Canonical Allele Identifier: PA916015153
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 526323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Gln1245Lys
CA8251008
NM_001286167.3:c.3733C>A