Canonical Allele Identifier: PA2573283409
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1422476
ClinVar RCV Id: RCV001926152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gly296Val
CA5924237
NM_022725.4:c.887G>T