Canonical Allele Identifier: PA645428277
Gene: PER2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376949
ClinVar RCV Id: RCV000440899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073728.1:p.Cys1084Arg
CA2196877
NM_022817.3:c.3250T>C