Allele Registry

Canonical Allele Identifier: PA109286

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011330

RCV001390295

ClinVar Variation:

10584

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Arg191Cys	CA255340 NM_000133.4:c.571C>T