Canonical Allele Identifier: PA2826634258
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483885
ClinVar RCV Id: RCV000562657 RCV000630127 RCV004001067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg14Lys
CA073615
NM_001281494.2:c.41G>A