Allele Registry

Canonical Allele Identifier: PA106033

Gene: F8 HGNC NCBI

ClinVar Allele:

25290

ClinVar RCV:

RCV000010964

RCV000601703

RCV002247322

ClinVar Variation:

10251

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Glu1057Lys	CA255144 NM_000132.4:c.3169G>A