Canonical Allele Identifier: PA2825051169
Gene: F9 HGNC NCBI
ClinVar RCV:
RCV001001440
ClinVar Variation:
811523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Cys64Arg
CA336130710
NM_000133.4:c.190T>C