Allele Registry

Canonical Allele Identifier: PA255407

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011363

ClinVar Variation:

10617

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Ser406Leu	CA255405 NM_000133.4:c.1217C>T