Allele Registry

Canonical Allele Identifier: PA2826946905

Gene: F9 HGNC NCBI

ClinVar Allele:

25624

ClinVar RCV:

RCV000011331

RCV000851602

RCV001390296

RCV002247326

RCV002284168

ClinVar Variation:

10585

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Arg153His	CA255342 NM_001313913.2:c.458G>A