Allele Registry

Canonical Allele Identifier: PA104744

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000852151

RCV003509601

ClinVar Variation:

627328

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg1768His	CA10568007 NM_000132.4:c.5303G>A