Canonical Allele Identifier: PA2826626288
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gln442Glu
CA346748599
NM_001281492.2:c.1324C>G