Allele Registry

Canonical Allele Identifier: PA915957915

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV000853373

RCV003156298

RCV003514423

ClinVar Variation:

692073

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Arg596Gln	CA380259622 NM_000506.5:c.1787G>A