Allele Registry

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Canonical Allele Identifier: PA658680799

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455171

ClinVar RCV Id: RCV000528067 RCV000580603 RCV001192423 RCV003153675

ClinVar Variation Id: 838100

ClinVar RCV Id: RCV001039583 RCV002416339

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Asp667Glu	CA346750666 NM_000179.3:c.2001T>G CA346750667 NM_000179.3:c.2001T>A