Canonical Allele Identifier: PA2826174594
Gene: SIRT6 HGNC NCBI

Linked Data

ClinVar Variation Id: 207888
ClinVar RCV Id: RCV000190172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180214.1:p.Arg221Cys
CA204145
NM_001193285.3:c.661C>T