Canonical Allele Identifier: PA916010901
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821829
ClinVar RCV Id: RCV001016638 RCV001873278
ClinVar Variation Id: 1793635
ClinVar RCV Id: RCV002426218
ClinVar Variation Id: 1796171
ClinVar RCV Id: RCV002441545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser9Arg
CA346734504
NM_001281492.2:c.25A>C
CA346734509
NM_001281492.2:c.27C>A
CA346734510
NM_001281492.2:c.27C>G