Allele Registry

Canonical Allele Identifier: PA2826947110

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011366

ClinVar Variation:

10620

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Pro376Thr	CA255411 NM_001313913.2:c.1126C>A