Allele Registry

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Canonical Allele Identifier: PA658747962

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491935

ClinVar RCV Id: RCV000581149 RCV002529260

ClinVar Variation Id: 863899

ClinVar RCV Id: RCV001070970 RCV002451308 RCV004000196

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Cys1098Ser	CA346758431 NM_000179.3:c.3292T>A CA346758448 NM_000179.3:c.3293G>C