Canonical Allele Identifier: PA2826624940
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1352094
ClinVar RCV Id: RCV002047340 RCV002388706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp123His
CA346740143
NM_001281492.2:c.367G>C