Canonical Allele Identifier: PA2826636738
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186654
ClinVar RCV Id: RCV000166282 RCV002515161
ClinVar Variation Id: 1024541
ClinVar RCV Id: RCV001324741 RCV001524726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp634Glu
CA010934
NM_001281494.2:c.1902T>G
CA346755613
NM_001281494.2:c.1902T>A