Allele Registry

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Canonical Allele Identifier: PA2499229315

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1005217

ClinVar RCV Id: RCV001302052

ClinVar Variation Id: 1716005

ClinVar RCV Id: RCV002295792

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly162Arg	CA346738612 NM_000179.3:c.484G>C CA346738614 NM_000179.3:c.484G>A