Canonical Allele Identifier: PA2826624919
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455344
ClinVar RCV Id: RCV000552704 RCV000777228 RCV004003703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg119Thr
CA346740105
NM_001281492.2:c.356G>C