Allele Registry

Canonical Allele Identifier: PA108162

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010990

ClinVar Variation:

10277

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Ser1803Tyr	CA255165 NM_000132.4:c.5408C>A