Allele Registry

Canonical Allele Identifier: PA2826626907

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160678

RCV000212658

RCV000542696

RCV001174633

RCV003467252

ClinVar Variation:

182633

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser584Cys	CA009720 NM_001281492.2:c.1751C>G