Canonical Allele Identifier: PA2826625096
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 656029
ClinVar RCV Id: RCV000812334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu160Arg
CA346740628
NM_001281492.2:c.479T>G