Canonical Allele Identifier: PA110495
Gene: F9 HGNC NCBI
ClinVar RCV:
RCV000011372
ClinVar Variation:
10628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Trp453Arg
CA255422
NM_000133.4:c.1357T>C
CA414447520
NM_000133.4:c.1357T>A