Allele Registry

Canonical Allele Identifier: PA108448

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010995

ClinVar Variation:

10282

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Thr1845Pro	CA255171 NM_000132.4:c.5533A>C