ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826946993
Gene: F9
HGNC
NCBI
Linked Data
ClinVar Variation Id:
10603
ClinVar RCV Id:
RCV000011349
RCV001001417
RCV002512971
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001300842.1:p.Arg260Ter