Canonical Allele Identifier: PA2826625210
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys187Glu
CA346740815
NM_001281492.2:c.559A>G