Allele Registry

Canonical Allele Identifier: PA106218

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010922

ClinVar Variation:

10209

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Glu409Gly	CA255099 NM_000132.4:c.1226A>G