Allele Registry

Canonical Allele Identifier: PA3057727098

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV005412183

ClinVar Variation:

3899330

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Gly121Asp	CA414919924 NM_000132.4:c.362G>A