Canonical Allele Identifier: PA2826633402
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 584622
ClinVar RCV Id: RCV000708891 RCV003353003 RCV001861936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr903dup
CA891843276
NM_001281493.2:c.2707_2709dup