Canonical Allele Identifier: PA2826625106
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1020877
ClinVar RCV Id: RCV001320534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro163Arg
CA346740663
NM_001281492.2:c.488C>G