Canonical Allele Identifier: PA2826627322
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676817
ClinVar RCV Id: RCV003461949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu682Val
CA346754036
NM_001281492.2:c.2044C>G