Allele Registry

Canonical Allele Identifier: PA109524

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011322

ClinVar Variation:

10576

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Asp93Gly	CA255322 NM_000133.4:c.278A>G