Allele Registry

Canonical Allele Identifier: PA255465

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011413

ClinVar Variation:

10660

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Arg384Pro	CA255463 NM_000133.4:c.1151G>C