Allele Registry

Canonical Allele Identifier: PA107299

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010866

ClinVar Variation:

10153

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Leu26Arg	CA255046 NM_000132.4:c.77T>G