Allele Registry

Canonical Allele Identifier: PA2826947062

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011385

RCV001001418

ClinVar Variation:

10639

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Val336Phe	CA255427 NM_001313913.2:c.1006G>T