Allele Registry

Canonical Allele Identifier: PA2826625146

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129487

RCV000168210

RCV000216085

RCV000589579

RCV000662957

RCV000708859

ClinVar Variation:

141122

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg172Thr	CA016638 NM_001281492.2:c.515G>C