Allele Registry

Canonical Allele Identifier: PA916011251

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000216842

RCV000227272

RCV000503628

RCV001080207

RCV003330587

RCV003997803

ClinVar Variation:

230117

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Val897Leu	CA10578129 NM_001281492.2:c.2689G>C CA346756559 NM_001281492.2:c.2689G>T