Canonical Allele Identifier: PA1139754357
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 970279
ClinVar RCV Id: RCV001245827 RCV002484370
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Arg122Gly
CA5924358
NM_022725.4:c.364C>G