Allele Registry

Canonical Allele Identifier: PA105791

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011064

ClinVar Variation:

10351

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Cys198Gly	CA255227 NM_000132.4:c.592T>G