Allele Registry

Canonical Allele Identifier: PA913191697

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000756124

ClinVar Variation:

618113

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Asp2093Val	CA414900400 NM_000132.4:c.6278A>T