Canonical Allele Identifier: PA2826624910
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2109024
ClinVar RCV Id: RCV003019898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys117Thr
CA346740082
NM_001281492.2:c.350A>C