Allele Registry

Canonical Allele Identifier: PA105676

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010934

ClinVar Variation:

10221

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Asp544Asn	CA255111 NM_000132.4:c.1630G>A