Canonical Allele Identifier: PA2826587089
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 861653
ClinVar RCV Id: RCV002355092 RCV001068220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg1016Lys
CA46719858
NM_001281494.2:c.3047G>A