Allele Registry

Canonical Allele Identifier: PA2826636388

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000568833

RCV001297702

RCV003998720

ClinVar Variation:

237161

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Asp555Asn	CA069199 NM_001281494.2:c.1663G>A