Allele Registry

Canonical Allele Identifier: PA2826947069

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011360

RCV003764552

ClinVar Variation:

10614

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Cys344Arg	CA255396 NM_001313913.2:c.1030T>C