Allele Registry

Canonical Allele Identifier: PA2826946928

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV002127085

ClinVar Variation:

1596936

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Val189Ile	CA10529819 NM_001313913.2:c.565G>A