Canonical Allele Identifier: PA2826626739
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2701387
ClinVar RCV Id: RCV003594910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu545_Ser547delinsGly
CA2697548152
NM_001281492.2:c.1634_1639del