Canonical Allele Identifier: PA2826630190
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233298
ClinVar RCV Id: RCV000223504 RCV000456959 RCV000486815 RCV003469073 RCV003998047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg166Pro
CA10578069
NM_001281493.2:c.497G>C