Allele Registry

Canonical Allele Identifier: PA2826947149

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV001000160

ClinVar Variation:

810865

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Ile416Thr	CA414447553 NM_001313913.2:c.1247T>C