Allele Registry

Canonical Allele Identifier: PA2826626913

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 560769

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Asp585Glu	CA346751088 NM_001281492.2:c.1755C>A CA346751090 NM_001281492.2:c.1755C>G