Allele Registry

Canonical Allele Identifier: PA2826947039

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011355

ClinVar Variation:

10609

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Gly317Val	CA255386 NM_001313913.2:c.950G>T