Allele Registry

Canonical Allele Identifier: PA255385

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011354

RCV003764551

ClinVar Variation:

10608

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Val353Ala	CA255383 NM_000133.4:c.1058T>C