Allele Registry

Canonical Allele Identifier: PA916011530

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000524174

RCV000573399

RCV001800369

RCV003460682

RCV003997088

ClinVar Variation:

89378

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Tyr998Cys	CA012724 NM_001281492.2:c.2993A>G