Allele Registry

Canonical Allele Identifier: PA2826947075

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011413

ClinVar Variation:

10660

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Arg346Pro	CA255463 NM_001313913.2:c.1037G>C