Canonical Allele Identifier: PA2826947148
Gene: F9 HGNC NCBI
ClinVar RCV:
RCV000011372
ClinVar Variation:
10628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Trp415Arg
CA255422
NM_001313913.2:c.1243T>C
CA414447520
NM_001313913.2:c.1243T>A