Canonical Allele Identifier: PA293898
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89245
ClinVar RCV Id: RCV000074709 RCV000128865 RCV000212657 RCV000524130 RCV000583928 RCV000576301 RCV001353773 RCV001526863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly686Asp
CA009620
NM_000179.3:c.2057G>A