Allele Registry

Canonical Allele Identifier: PA2826628103

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000563188

RCV001056457

RCV001293522

RCV004001053

ClinVar Variation:

483787

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu865Gln	CA346756363 NM_001281492.2:c.2593G>C