Canonical Allele Identifier: PA2825089080
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784018
ClinVar RCV Id: RCV002416955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu665Gln
CA346750653
NM_000179.3:c.1993G>C