Allele Registry

Canonical Allele Identifier: PA097331

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV002468924

ClinVar Variation:

13303

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Arg314Cys	CA123003 NM_000506.5:c.940C>T