Canonical Allele Identifier: PA2825091183
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730489
ClinVar RCV Id: RCV002320957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Cys1117Gly
CA346758754
NM_000179.3:c.3349T>G