Allele Registry

Canonical Allele Identifier: PA108521

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010903

ClinVar Variation:

10190

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Thr294Ile	CA255077 NM_000132.4:c.881C>T