Allele Registry

Canonical Allele Identifier: PA108903

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010926

ClinVar Variation:

10213

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Tyr450Asn	CA255103 NM_000132.4:c.1348T>A