Canonical Allele Identifier: PA2826635698
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 820658
ClinVar RCV Id: RCV001014331 RCV001211376 RCV002268403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys390Gln
CA068450
NM_001281494.2:c.1168A>C