Canonical Allele Identifier: PA204146
Gene: SIRT6 HGNC NCBI

Linked Data

ClinVar Variation Id: 207888
ClinVar RCV Id: RCV000190172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057623.2:p.Arg248Cys
CA204145
NM_016539.3:c.742C>T