Allele Registry

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Canonical Allele Identifier: PA2825087190

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567482

ClinVar RCV Id: RCV003759811 RCV003311264

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser292Arg	CA346740646 NM_000179.3:c.874A>C CA346740655 NM_000179.3:c.876C>A CA346740656 NM_000179.3:c.876C>G