Allele Registry

Canonical Allele Identifier: PA111778

Gene: PER2 HGNC NCBI

ClinVar Allele:

21384

ClinVar RCV:

RCV000006717

ClinVar Variation:

6345

HGVS (amino-acid)	Matching Registered Transcripts
NP_073728.1:p.Ser662Gly	CA118132 NM_022817.3:c.1984A>G