Canonical Allele Identifier: PA2826627629
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1482874
ClinVar RCV Id: RCV002025284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile756Thr
CA346755187
NM_001281492.2:c.2267T>C