Allele Registry

Canonical Allele Identifier: PA2826946998

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011350

ClinVar Variation:

10604

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Asn268Ser	CA255373 NM_001313913.2:c.803A>G