Allele Registry

Canonical Allele Identifier: PA915958775

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV001002603

ClinVar Variation:

116175

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Cys382Ser	CA336143348 NM_000133.4:c.1144T>A CA414446165 NM_000133.4:c.1145G>C