Canonical Allele Identifier: PA2826625721
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1433974
ClinVar RCV Id: RCV001952767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Tyr306His
CA346744316
NM_001281492.2:c.916T>C