Allele Registry

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Canonical Allele Identifier: PA891846094

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 582516

ClinVar RCV Id: RCV000706608

ClinVar Variation Id: 1403905

ClinVar RCV Id: RCV001898894 RCV002344002 RCV003442947

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Val398Leu	CA067302 NM_000179.3:c.1192G>T CA346743374 NM_000179.3:c.1192G>C