Canonical Allele Identifier: PA645431694
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 435151
ClinVar RCV Id: RCV000500151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Val177Met
CA5924315
NM_022725.4:c.529G>A