Allele Registry

Canonical Allele Identifier: PA2826627554

Gene: MSH6 HGNC NCBI

ClinVar Allele:

392936

ClinVar RCV:

RCV000464988

RCV000771517

RCV001798840

RCV002289613

RCV004000830

ClinVar Variation:

410399

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Met738Thr	CA069266 NM_001281492.2:c.2213T>C