Canonical Allele Identifier: PA2825087541
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1768617
ClinVar RCV Id: RCV002382834 RCV003094898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser331Thr
CA346741104
NM_000179.3:c.991T>A