Canonical Allele Identifier: PA2826628860
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 945402
ClinVar RCV Id: RCV001216034 RCV003142159 RCV003363173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr1113Ala
CA071913
NM_001281492.2:c.3337A>G