Allele Registry

Canonical Allele Identifier: PA105388

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010904

ClinVar Variation:

10191

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Asn299Ile	CA255078 NM_000132.4:c.896A>T