Allele Registry

Canonical Allele Identifier: PA2826947074

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011414

RCV000119810

ClinVar Variation:

10668

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Arg346Leu	CA121138 NM_001313913.2:c.1037G>T