Allele Registry

Canonical Allele Identifier: PA2826947137

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011368

ClinVar Variation:

10622

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Ala398Glu	CA255413 NM_001313913.2:c.1193C>A