Canonical Allele Identifier: PA2826635498
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023786
ClinVar RCV Id: RCV001323891
ClinVar Variation Id: 1783109
ClinVar RCV Id: RCV002413236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser346Arg
CA346750466
NM_001281494.2:c.1036A>C
CA346750486
NM_001281494.2:c.1038T>A
CA346750489
NM_001281494.2:c.1038T>G