Allele Registry

Canonical Allele Identifier: PA105126

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010823

RCV000757254

RCV000852002

ClinVar Variation:

10111

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg391His	CA120918 NM_000132.4:c.1172G>A