Canonical Allele Identifier: PA2826626706
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455171
ClinVar RCV Id: RCV000528067 RCV000580603 RCV001192423 RCV003153675
ClinVar Variation Id: 838100
ClinVar RCV Id: RCV001039583 RCV002416339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp537Glu
CA346750666
NM_001281492.2:c.1611T>G
CA346750667
NM_001281492.2:c.1611T>A