Canonical Allele Identifier: PA2826628563
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1732521
ClinVar RCV Id: RCV002337616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg1052Lys
CA346760253
NM_001281492.2:c.3155G>A