Canonical Allele Identifier: PA2573095357
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1343704
ClinVar RCV Id: RCV001844721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Val302Met
CA380058091
NM_022725.4:c.904G>A