Canonical Allele Identifier: PA2826631903
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141589
ClinVar RCV Id: RCV000130173 RCV000222583 RCV000238642 RCV000524147 RCV003317097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val565Gly
CA010487
NM_001281493.2:c.1694T>G