Canonical Allele Identifier: PA2573192161
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1520225
ClinVar RCV Id: RCV002038581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser97Arg
CA346739870
NM_001281492.2:c.289A>C
CA346739883
NM_001281492.2:c.291T>A
CA346739887
NM_001281492.2:c.291T>G