Canonical Allele Identifier: PA2826625171
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1766268
ClinVar RCV Id: RCV002371322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly178Cys
CA346740743
NM_001281492.2:c.532G>T