Canonical Allele Identifier: PA2826628831
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1039964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr1108Pro
CA46719365
NM_001281492.2:c.3322A>C