Allele Registry

Canonical Allele Identifier: PA106319

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010986

ClinVar Variation:

10273

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Gly1779Glu	CA255161 NM_000132.4:c.5336G>A