Canonical Allele Identifier: PA2741983519
Gene: PER2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2652064
ClinVar RCV Id: RCV003440269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073728.1:p.Pro8Leu
CA2197911
NM_022817.3:c.23C>T