Canonical Allele Identifier: PA2826629171
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185639
ClinVar RCV Id: RCV000165091
ClinVar Variation Id: 1365015
ClinVar RCV Id: RCV001907789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg1174Ser
CA014672
NM_001281492.2:c.3522G>T
CA346761443
NM_001281492.2:c.3522G>C