Canonical Allele Identifier: PA2827069387
Gene: SIRT6 HGNC NCBI

Linked Data

ClinVar Variation Id: 207888
ClinVar RCV Id: RCV000190172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307987.1:p.Arg176Cys
CA204145
NM_001321058.2:c.526C>T