Canonical Allele Identifier: PA2826627390
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 140892
ClinVar RCV Id: RCV000129131 RCV000226891 RCV001140447 RCV003997483 RCV004532546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val698Ile
CA010298
NM_001281492.2:c.2092G>A