Allele Registry

Canonical Allele Identifier: PA2826947070

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV001002603

ClinVar Variation:

116175

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Cys344Ser	CA336143348 NM_001313913.2:c.1030T>A CA414446165 NM_001313913.2:c.1031G>C