Allele Registry

Canonical Allele Identifier: PA106483

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010893

ClinVar Variation:

10180

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Gly224Trp	CA255069 NM_000132.4:c.670G>T