Allele Registry

Canonical Allele Identifier: PA105239

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010938

RCV003656622

ClinVar Variation:

10225

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg550His	CA255115 NM_000132.4:c.1649G>A