Canonical Allele Identifier: PA2826636950
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410482
ClinVar RCV Id: RCV002230416 RCV002436447 RCV004001842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg686Pro
CA069882
NM_001281494.2:c.2057G>C