Canonical Allele Identifier: PA2826629030
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2806770
ClinVar RCV Id: RCV003760747 RCV004371637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser1149Ile
CA346761284
NM_001281492.2:c.3446G>T