Allele Registry

Canonical Allele Identifier: PA2826626290

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002398956

ClinVar Variation:

1778619

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gln442Arg	CA346748606 NM_001281492.2:c.1325A>G