Canonical Allele Identifier: PA2826627540
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 140829
ClinVar RCV Id: RCV000129021 RCV000557524 RCV003997471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly734Glu
CA010461
NM_001281492.2:c.2201G>A