Allele Registry

Canonical Allele Identifier: PA104854

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010841

ClinVar Variation:

10128

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg2135Pro	CA255029 NM_000132.4:c.6404G>C