ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2573283393
Gene: FANCF
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1375139
ClinVar RCV Id:
RCV001879522
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_073562.1:p.Tyr274Cys
CA5924253
NM_022725.4:c.821A>G