Canonical Allele Identifier: PA916011164
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu98Lys
CA016246
NM_001281492.2:c.292G>A