Allele Registry

Canonical Allele Identifier: PA109503

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011389

ClinVar Variation:

10643

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Asp110Asn	CA255435 NM_000133.4:c.328G>A