Allele Registry

Canonical Allele Identifier: PA107902

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010994

RCV000851817

ClinVar Variation:

10281

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Pro1844Ser	CA255170 NM_000132.4:c.5530C>T