Canonical Allele Identifier: PA2826624929
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1759382
ClinVar RCV Id: RCV002393882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile121Thr
CA346740130
NM_001281492.2:c.362T>C