Canonical Allele Identifier: PA2826626740
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu545Lys
CA10582057
NM_001281492.2:c.1633G>A