Canonical Allele Identifier: PA2826631898
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479962
ClinVar RCV Id: RCV000568107 RCV000629749 RCV004000887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys564Glu
CA346754894
NM_001281493.2:c.1690A>G