Allele Registry

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Canonical Allele Identifier: PA2826626076

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1775540

ClinVar RCV Id: RCV002392620

JSON-LD

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser395Arg	CA346746803 NM_001281492.2:c.1183A>C CA346746821 NM_001281492.2:c.1185T>A CA346746822 NM_001281492.2:c.1185T>G