Canonical Allele Identifier: PA2826629205
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89482
ClinVar RCV Id: RCV000129017 RCV000524194 RCV001548132 RCV001804807 RCV003997097
ClinVar Variation Id: 863587
ClinVar RCV Id: RCV001070583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1180Asp
CA014716
NM_001281492.2:c.3540G>C
CA346761480
NM_001281492.2:c.3540G>T