Canonical Allele Identifier: PA2826627265
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790593
ClinVar RCV Id: RCV002459593 RCV003759731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu668Pro
CA346753867
NM_001281492.2:c.2003T>C