Canonical Allele Identifier: PA2826626844
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485863
ClinVar RCV Id: RCV000569729 RCV001853779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gln568Arg
CA346750872
NM_001281492.2:c.1703A>G