Allele Registry

Canonical Allele Identifier: PA106306

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010983

ClinVar Variation:

10270

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Gly1769Arg	CA255158 NM_000132.4:c.5305G>A CA414910833 NM_000132.4:c.5305G>C