Canonical Allele Identifier: PA2826635671
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89245
ClinVar RCV Id: RCV000074709 RCV000128865 RCV000212657 RCV000524130 RCV000583928 RCV000576301 RCV001353773 RCV001526863
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly384Asp
CA009620
NM_001281494.2:c.1151G>A