Allele Registry

Canonical Allele Identifier: PA108833

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011023

RCV001508071

ClinVar Variation:

10310

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Tyr2124Cys	CA255203 NM_000132.4:c.6371A>G