Canonical Allele Identifier: PA2826625132
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2099257
ClinVar RCV Id: RCV003021628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys169Met
CA346740696
NM_001281492.2:c.506A>T