Allele Registry

Canonical Allele Identifier: PA123021

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV002468930

ClinVar Variation:

13312

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Glu352Lys	CA123019 NM_000506.5:c.1054G>A