Allele Registry

Canonical Allele Identifier: PA110058

Gene: F9 HGNC NCBI

ClinVar Allele:

25663

ClinVar RCV:

RCV000011370

ClinVar Variation:

10624

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Gly442Arg	CA255418 NM_000133.4:c.1324G>A CA414447344 NM_000133.4:c.1324G>C