Allele Registry

Canonical Allele Identifier: PA2826947084

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011362

ClinVar Variation:

10616

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Met356Val	CA255402 NM_001313913.2:c.1066A>G