Allele Registry

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Canonical Allele Identifier: PA2573163435

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1514670

ClinVar RCV Id: RCV002029468

ClinVar Variation Id: 1783420

ClinVar RCV Id: RCV002421729

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Met654Leu	CA346750579 NM_000179.3:c.1960A>T CA346750581 NM_000179.3:c.1960A>C