Canonical Allele Identifier: PA2499289387
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1002405
ClinVar RCV Id: RCV001298825 RCV002499550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Met145Val
CA219086644
NM_022725.4:c.433A>G