Canonical Allele Identifier: PA2826625130
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765273
ClinVar RCV Id: RCV002449906 RCV003100068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys169Arg
CA346740695
NM_001281492.2:c.506A>G