Canonical Allele Identifier: PA2826633537
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 824098
ClinVar RCV Id: RCV001020925 RCV003314658 RCV003758984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu932Gln
CA46719355
NM_001281493.2:c.2794G>C