Allele Registry

Canonical Allele Identifier: PA2826947076

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV001266976

RCV003313792

ClinVar Variation:

985854

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Arg346Gln	CA414446196 NM_001313913.2:c.1037G>A