Canonical Allele Identifier: PA2827069492
Gene: SIRT6 HGNC NCBI

Linked Data

ClinVar Variation Id: 207888
ClinVar RCV Id: RCV000190172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307990.1:p.Arg149Cys
CA204145
NM_001321061.1:c.445C>T