Allele Registry

Canonical Allele Identifier: PA097347

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV002468926

ClinVar Variation:

13305

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Arg425Cys	CA123007 NM_000506.5:c.1273C>T