Canonical Allele Identifier: PA2826587086
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 845670
ClinVar RCV Id: RCV001048782 RCV002374893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg1016Gly
CA346761525
NM_001281494.2:c.3046A>G