Allele Registry

Canonical Allele Identifier: PA123027

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV002468932

ClinVar Variation:

13314

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Asp595Glu	CA123025 NM_000506.5:c.1785C>G CA380259619 NM_000506.5:c.1785C>A