Canonical Allele Identifier: PA2826627702
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89309
ClinVar RCV Id: RCV000559913 RCV000570122 RCV001561918 RCV003460671 RCV003997081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg771His
CA010764
NM_001281492.2:c.2312G>A