Allele Registry

Canonical Allele Identifier: PA105109

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010906

ClinVar Variation:

10193

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg301Leu	CA255080 NM_000132.4:c.902G>T