Allele Registry

Canonical Allele Identifier: PA2826627143

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000481556

RCV000822224

RCV001190572

RCV003470572

RCV004003355

ClinVar Variation:

421501

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro638Ala	CA068796 NM_001281492.2:c.1912C>G