Canonical Allele Identifier: PA2826627726
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 489991
ClinVar Variation Id: 2567462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr776Ser
CA346755348
NM_001281492.2:c.2326A>T
CA346755351
NM_001281492.2:c.2327C>G