Allele Registry

Canonical Allele Identifier: PA2826631891

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 140829

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gly562Glu	CA010461 NM_001281493.2:c.1685G>A