Allele Registry

Canonical Allele Identifier: PA110372

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011366

ClinVar Variation:

10620

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Pro414Thr	CA255411 NM_000133.4:c.1240C>A