Allele Registry

Canonical Allele Identifier: PA2826947089

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011388

RCV001000171

ClinVar Variation:

10642

810871

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Cys358Ser	CA255433 NM_001313913.2:c.1073G>C CA414446364 NM_001313913.2:c.1072T>A