Canonical Allele Identifier: PA2826626800
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1356583
ClinVar RCV Id: RCV001876763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Cys557Phe
CA346750774
NM_001281492.2:c.1670G>T