Canonical Allele Identifier: PA2741983521
Gene: PER2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2591672
ClinVar RCV Id: RCV004339494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073728.1:p.Pro72Ser
CA2197877
NM_022817.3:c.214C>T