Allele Registry

Canonical Allele Identifier: PA110571

Gene: F9 HGNC NCBI

ClinVar Allele:

649734

ClinVar RCV:

RCV000806960

ClinVar Variation:

651569

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Val30Ile	CA414434500 NM_000133.4:c.88G>A