Allele Registry

Canonical Allele Identifier: PA645509717

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV003654415

ClinVar Variation:

439677

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Gly1729Glu	CA414913556 NM_000132.4:c.5186G>A