Allele Registry

Canonical Allele Identifier: PA916021261

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011317

ClinVar Variation:

10571

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Glu73Val	CA255316 NM_001313913.2:c.218A>T