Canonical Allele Identifier: PA2826633342
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu891Lys
CA013478
NM_001281493.2:c.2671G>A