Allele Registry

Canonical Allele Identifier: PA2573162459

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV002127085

ClinVar Variation:

1596936

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Val227Ile	CA10529819 NM_000133.4:c.679G>A