Canonical Allele Identifier: PA2741983542
Gene: PER2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3043837
ClinVar RCV Id: RCV003937030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073728.1:p.Ala664Val
CA2197218
NM_022817.3:c.1991C>T