Canonical Allele Identifier: PA916015216
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 656395
ClinVar RCV Id: RCV000812802
ClinVar Variation Id: 803291
ClinVar RCV Id: RCV000989669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Gln1389His
CA397484248
NM_001286167.3:c.4167G>T
CA397484249
NM_001286167.3:c.4167G>C