Canonical Allele Identifier: PA2825087888
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 818513
ClinVar RCV Id: RCV001010181 RCV001819721 RCV001296294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser394Cys
CA346742378
NM_000179.3:c.1181C>G