Canonical Allele Identifier: PA159586
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 134355
ClinVar RCV Id: RCV000121029 RCV000457324
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gly243Glu
CA159584
NM_022725.4:c.728G>A