Canonical Allele Identifier: PA2826625188
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1766677
ClinVar RCV Id: RCV002371707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg182Lys
CA346740762
NM_001281492.2:c.545G>A