Allele Registry

Canonical Allele Identifier: PA2826635300

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001036600

RCV003160216

ClinVar Variation:

835660

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu302Lys	CA346749379 NM_001281494.2:c.904G>A