Canonical Allele Identifier: PA2826634787
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142768
ClinVar RCV Id: RCV000132161 RCV000203804 RCV000480825 RCV003998134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu182Gln
CA008646
NM_001281494.2:c.544G>C