Allele Registry

Canonical Allele Identifier: PA2826626288

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491403

RCV001204099

ClinVar Variation:

428315

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gln442Glu	CA346748599 NM_001281492.2:c.1324C>G