Canonical Allele Identifier: PA2573283397
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1391665
ClinVar RCV Id: RCV001881997
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gln283His
CA380058205
NM_022725.4:c.849A>T
CA380058206
NM_022725.4:c.849A>C