Canonical Allele Identifier: PA2830011196
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 3092808
ClinVar RCV Id: RCV004383725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gly150Ser
CA219086643
NM_022725.4:c.448G>A