Canonical Allele Identifier: PA2826631528
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587343
ClinVar RCV Id: RCV003360821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu476Pro
CA346753385
NM_001281493.2:c.1427T>C