Allele Registry

Canonical Allele Identifier: PA2826947101

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011363

ClinVar Variation:

10617

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Ser368Leu	CA255405 NM_001313913.2:c.1103C>T