Allele Registry

Canonical Allele Identifier: PA2826947014

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV003388353

ClinVar Variation:

2627159

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Pro286His	CA414445085 NM_001313913.2:c.857C>A