Allele Registry

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Canonical Allele Identifier: PA2826637291

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567451

ClinVar RCV Id: RCV003311248

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ser765Arg	CA346757863 NM_001281494.2:c.2293A>C CA346757876 NM_001281494.2:c.2295T>G CA346757878 NM_001281494.2:c.2295T>A