Allele Registry

Canonical Allele Identifier: PA255398

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011360

RCV003764552

ClinVar Variation:

10614

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Cys382Arg	CA255396 NM_000133.4:c.1144T>C