Canonical Allele Identifier: PA255377
Gene: F9 HGNC NCBI
ClinVar RCV:
RCV000011351
ClinVar Variation:
10605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Pro333Leu
CA255375
NM_000133.4:c.998C>T