Canonical Allele Identifier: PA2573283389
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1691930
ClinVar RCV Id: RCV002258417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Ser271Phe
CA380058277
NM_022725.4:c.812C>T