Allele Registry

Canonical Allele Identifier: PA108864

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011065

ClinVar Variation:

10352

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Tyr35Cys	CA255228 NM_000132.4:c.104A>G