Allele Registry

Canonical Allele Identifier: PA105055

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010821

ClinVar Variation:

10109

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg2326Leu	CA255018 NM_000132.4:c.6977G>T