Allele Registry

Canonical Allele Identifier: PA2826625050

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000531362

RCV000579639

RCV004003706

ClinVar Variation:

455353

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly151Val	CA073491 NM_001281492.2:c.452G>T