Allele Registry

Canonical Allele Identifier: PA2826632862

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000122963

RCV000128933

RCV000411062

RCV000587527

RCV001255217

RCV001354177

RCV003149837

ClinVar Variation:

135841

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Pro785Ala	CA012231 NM_001281493.2:c.2353C>G