Canonical Allele Identifier: PA1139754324
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 943823
ClinVar RCV Id: RCV001214094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Arg108Cys
CA5924373
NM_022725.4:c.322C>T