Allele Registry

Canonical Allele Identifier: PA109372

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011414

RCV000119810

ClinVar Variation:

10668

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Arg384Leu	CA121138 NM_000133.4:c.1151G>T