Canonical Allele Identifier: PA2826635617
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444000
ClinVar RCV Id: RCV001981571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu373Gln
CA346750704
NM_001281494.2:c.1117G>C