Canonical Allele Identifier: PA2826628668
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 934973
ClinVar RCV Id: RCV001203471 RCV004033573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His1073Arg
CA346760564
NM_001281492.2:c.3218A>G