Allele Registry

Canonical Allele Identifier: PA916071849

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011027

ClinVar Variation:

10314

HGVS (amino-acid)	Matching Registered Transcripts
NP_063916.1:p.Arg43Leu	CA255207 NM_019863.3:c.128G>T