Canonical Allele Identifier: PA2580456788
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2145566
ClinVar RCV Id: RCV003071503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Trp281Arg
CA380058225
NM_022725.4:c.841T>A
CA380058226
NM_022725.4:c.841T>C