Allele Registry

Canonical Allele Identifier: PA2826626515

Gene: MSH6 HGNC NCBI

ClinVar Allele:

232733

ClinVar RCV:

RCV000217487

RCV000464191

RCV000480702

RCV001293521

RCV003998588

ClinVar Variation:

233917

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly494Val	CA068227 NM_001281492.2:c.1481G>T