Canonical Allele Identifier: PA2826625136
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 933184
ClinVar RCV Id: RCV001201240 RCV001201716 RCV002375126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg170Pro
CA46706922
NM_001281492.2:c.509G>C