Canonical Allele Identifier: PA2826627053
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr620Lys
CA009894
NM_001281492.2:c.1859C>A