Allele Registry

Canonical Allele Identifier: PA2829907310

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010839

RCV000851861

RCV001169905

ClinVar Variation:

10126

HGVS (amino-acid)	Matching Registered Transcripts
NP_063916.1:p.Arg191Gln	CA255027 NM_019863.3:c.572G>A