Allele Registry

Canonical Allele Identifier: PA2826628163

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003484586

RCV004364854

ClinVar Variation:

2683985

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu893Gln	CA346756538 NM_001281492.2:c.2677G>C