Allele Registry

Canonical Allele Identifier: PA109480

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011350

ClinVar Variation:

10604

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Asn306Ser	CA255373 NM_000133.4:c.917A>G