Canonical Allele Identifier: PA2580456762
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2088173
ClinVar RCV Id: RCV003009931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Ala208Glu
CA5924299
NM_022725.4:c.623C>A