Canonical Allele Identifier: PA2825092979
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1479666
ClinVar RCV Id: RCV001976889 RCV002352692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.[Glu1348_Lys1352delinsGln;Leu1354Ter]
CA2573134810
NM_000179.3:c.4028_4041dup