Canonical Allele Identifier: PA330629
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89568
ClinVar RCV Id: RCV000568144 RCV000684794 RCV000759873 RCV002267836 RCV002504983 RCV003997104
ClinVar Variation Id: 479870
ClinVar RCV Id: RCV000564981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr269Ser
CA016470
NM_000179.3:c.806C>G
CA346740355
NM_000179.3:c.805A>T