Allele Registry

Canonical Allele Identifier: PA916011475

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000582580

RCV000808125

RCV004002352

ClinVar Variation:

491937

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Asp977Glu	CA346758673 NM_001281492.2:c.2931T>G CA346758674 NM_001281492.2:c.2931T>A