Allele Registry

Canonical Allele Identifier: PA2826635390

Gene: MSH6 HGNC NCBI

ClinVar Allele:

232733

ClinVar RCV:

RCV000217487

RCV000464191

RCV000480702

RCV001293521

RCV003998588

ClinVar Variation:

233917

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gly322Val	CA068227 NM_001281494.2:c.965G>T