Canonical Allele Identifier: PA916068809
Gene: PER2 HGNC NCBI

Linked Data

ClinVar Variation Id: 756161
ClinVar RCV Id: RCV000933637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073728.1:p.Pro72Leu
CA2197876
NM_022817.3:c.215C>T
CA645534867
NM_022817.3:c.214_215delinsTT