Allele Registry

Canonical Allele Identifier: PA109881

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011320

ClinVar Variation:

10574

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Glu79Asp	CA255320 NM_000133.4:c.237A>C CA414436237 NM_000133.4:c.237A>T