Canonical Allele Identifier: PA2826625145
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231964
ClinVar RCV Id: RCV000218110 RCV000629734 RCV001762489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg172Ile
CA10578051
NM_001281492.2:c.515G>T