Canonical Allele Identifier: PA2826946929
Gene: F9 HGNC NCBI
ClinVar RCV:
RCV003324302
ClinVar Variation:
2577225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Val190Ile
CA414441149
NM_001313913.2:c.568G>A