Allele Registry

Canonical Allele Identifier: PA2826636435

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000464988

RCV000771517

RCV001798840

RCV002289613

RCV004000830

ClinVar Variation:

410399

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Met566Thr	CA069266 NM_001281494.2:c.1697T>C