Allele Registry

Canonical Allele Identifier: PA105229

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010937

RCV000757245

ClinVar Variation:

10224

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg550Gly	CA255114 NM_000132.4:c.1648C>G