Allele Registry

Canonical Allele Identifier: PA255333

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011326

ClinVar Variation:

10580

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Asp110Gly	CA255331 NM_000133.4:c.329A>G