Canonical Allele Identifier: PA255336
Gene: F9 HGNC NCBI
ClinVar Allele:
25620
ClinVar RCV:
RCV000011327
ClinVar Variation:
10581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Gly160Ala
CA255334
NM_000133.4:c.479G>C