Allele Registry

Canonical Allele Identifier: PA109776

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011323

ClinVar Variation:

10577

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Gln96Pro	CA255324 NM_000133.4:c.287A>C