Canonical Allele Identifier: PA2826625406
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1350133
ClinVar RCV Id: RCV002039524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro232Ala
CA346741811
NM_001281492.2:c.694C>G