Allele Registry

Canonical Allele Identifier: PA107913

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011002

ClinVar Variation:

10289

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Pro1873Arg	CA255178 NM_000132.4:c.5618C>G