Canonical Allele Identifier: PA2826625185
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 449895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys181Glu
CA346740754
NM_001281492.2:c.541A>G