Canonical Allele Identifier: PA1139754439
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 848522
ClinVar RCV Id: RCV001052297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gly258Arg
CA5924263
NM_022725.4:c.772G>A
CA380058357
NM_022725.4:c.772G>C