Allele Registry

Canonical Allele Identifier: PA123018

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV002468929

ClinVar Variation:

13311

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Glu343Lys	CA123016 NM_000506.5:c.1027G>A