Allele Registry

Canonical Allele Identifier: PA2826947140

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011371

RCV001382695

RCV001810850

ClinVar Variation:

10627

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Ile405Thr	CA255420 NM_001313913.2:c.1214T>C