Canonical Allele Identifier: PA2580456784
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2132323
ClinVar RCV Id: RCV003036677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Asp280Tyr
CA380058232
NM_022725.4:c.838G>T