Canonical Allele Identifier: PA2826627028
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788028
ClinVar RCV Id: RCV002428173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu613Trp
CA346752486
NM_001281492.2:c.1838T>G