Allele Registry

Canonical Allele Identifier: PA916071867

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011035

ClinVar Variation:

10322

HGVS (amino-acid)	Matching Registered Transcripts
NP_063916.1:p.Ala76Pro	CA255215 NM_019863.3:c.226G>C