Allele Registry

Canonical Allele Identifier: PA916012305

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000130625

RCV000589175

RCV001086478

RCV001260255

RCV003998071

ClinVar Variation:

141916

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Pro976Thr	CA014466 NM_001281494.2:c.2926C>A