Allele Registry

Canonical Allele Identifier: PA105878

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010915

ClinVar Variation:

10202

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Cys348Ser	CA255091 NM_000132.4:c.1043G>C CA414917198 NM_000132.4:c.1042T>A