Allele Registry

Canonical Allele Identifier: PA109276

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011369

ClinVar Variation:

10623

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Ala436Val	CA255416 NM_000133.4:c.1307C>T