Allele Registry

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Canonical Allele Identifier: PA2826627127

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 801698

ClinVar RCV Id: RCV000986721 RCV001351789

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.His636Gln	CA068773 NM_001281492.2:c.1908T>G CA346753012 NM_001281492.2:c.1908T>A