Canonical Allele Identifier: PA1139690867
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 955698
ClinVar RCV Id: RCV001228382 RCV002259096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val890Ile
CA346760496
NM_001281494.2:c.2668G>A