Allele Registry

Canonical Allele Identifier: PA2826946972

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV001973941

ClinVar Variation:

1477908

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Ala241Pro	CA414443714 NM_001313913.2:c.721G>C