Allele Registry

Canonical Allele Identifier: PA106851

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000852165

ClinVar Variation:

627340

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.His1973Leu	CA414905984 NM_000132.4:c.5918A>T