Allele Registry

Canonical Allele Identifier: PA105581

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011000

ClinVar Variation:

10287

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Asp1865Tyr	CA255176 NM_000132.4:c.5593G>T