ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2573095351
Gene: FANCF
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1338057
ClinVar RCV Id:
RCV001822655
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_073562.1:p.Arg101Trp
CA5924378
NM_022725.4:c.301C>T