Canonical Allele Identifier: PA2826625148
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184781
ClinVar RCV Id: RCV000164096 RCV003758704 RCV003995313
ClinVar Variation Id: 643969
ClinVar RCV Id: RCV000797791 RCV002442640 RCV003338803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met173Ile
CA016648
NM_001281492.2:c.519G>T
CA346740716
NM_001281492.2:c.519G>A
CA346740717
NM_001281492.2:c.519G>C