ClinGen Allele Registry
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Canonical Allele Identifier:
PA110001
Gene: F9
HGNC
NCBI
Linked Data
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_000124.1:p.Gly357Arg
NM_000133.4:c.1069G>A
NM_000133.4:c.1069G>C