Allele Registry

Canonical Allele Identifier: PA106176

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010811

ClinVar Variation:

10099

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Glu291Gly	CA255017 NM_000132.4:c.872A>G