Allele Registry

Canonical Allele Identifier: PA2826947139

Gene: F9 HGNC NCBI

ClinVar Allele:

25663

ClinVar RCV:

RCV000011370

ClinVar Variation:

10624

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Gly404Arg	CA255418 NM_001313913.2:c.1210G>A CA414447344 NM_001313913.2:c.1210G>C