Canonical Allele Identifier: PA2826625762
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 935156
ClinVar RCV Id: RCV001203684 RCV002379769 RCV004010631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu316Lys
CA346744558
NM_001281492.2:c.946G>A