Canonical Allele Identifier: PA2830016354
Gene: PER2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3211436
ClinVar RCV Id: RCV004505824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073728.1:p.Pro71Ser
CA351266433
NM_022817.3:c.211C>T