Canonical Allele Identifier: PA2826637797
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2036675
ClinVar RCV Id: RCV002899323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.His946Arg
CA346761058
NM_001281494.2:c.2837A>G