Allele Registry

Canonical Allele Identifier: PA2826625062

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003044687

RCV004070114

ClinVar Variation:

2133945

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly153dup	CA073501 NM_001281492.2:c.458_460dup