Allele Registry

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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