Allele Registry

Canonical Allele Identifier: PA104829

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011017

ClinVar Variation:

10304

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg2016Trp	CA255197 NM_000132.4:c.6046C>T