Canonical Allele Identifier: PA2825086976
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1762113
ClinVar RCV Id: RCV002421318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu271Val
CA346740386
NM_000179.3:c.812A>T