Canonical Allele Identifier: PA2826624999
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_001268421.1:p.Thr139Ser
CA016470
NM_001281492.2:c.416C>G
CA346740355
NM_001281492.2:c.415A>T