Allele Registry

Canonical Allele Identifier: PA255339

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV000011328

ClinVar Variation:

10582

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Asn166Tyr	CA255337 NM_000133.4:c.496A>T