Allele Registry

Canonical Allele Identifier: PA097368

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV002468925

ClinVar Variation:

13304

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Arg461Trp	CA123005 NM_000506.5:c.1381C>T