Allele Registry

Canonical Allele Identifier: PA1139670918

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV001266976

RCV003313792

ClinVar Variation:

985854

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Arg384Gln	CA414446196 NM_000133.4:c.1151G>A