Allele Registry

Canonical Allele Identifier: PA107483

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010925

ClinVar Variation:

10212

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Lys444Arg	CA255102 NM_000132.4:c.1331A>G