Allele Registry

Canonical Allele Identifier: PA2826634837

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000560586

RCV000567174

RCV000680207

RCV004003662

ClinVar Variation:

455141

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Cys194Tyr	CA067747 NM_001281494.2:c.581G>A