Allele Registry

Canonical Allele Identifier: PA255388

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011355

ClinVar Variation:

10609

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Gly355Val	CA255386 NM_000133.4:c.1064G>T