Canonical Allele Identifier: PA109299
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10591
ClinVar RCV Id: RCV000011337 RCV001727513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Arg226Gln
CA121128
NM_000133.4:c.677G>A