Allele Registry

Canonical Allele Identifier: PA107097

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010862

ClinVar Variation:

10149

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Ile585Thr	CA255043 NM_000132.4:c.1754T>C