Allele Registry

Canonical Allele Identifier: PA916071865

Gene: F8 HGNC NCBI

ClinVar Allele:

348627

ClinVar RCV:

RCV000403190

RCV002252106

RCV003392221

ClinVar Variation:

368117

HGVS (amino-acid)	Matching Registered Transcripts
NP_063916.1:p.Gln73Arg	CA10567784 NM_019863.3:c.218A>G