Canonical Allele Identifier: PA2826637668
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1732527
ClinVar RCV Id: RCV003594197 RCV002454829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile881Val
CA346760259
NM_001281494.2:c.2641A>G