Allele Registry

Canonical Allele Identifier: PA2826636585

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000559913

RCV000570122

RCV001561918

RCV003460671

RCV003997081

ClinVar Variation:

89309

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg599His	CA010764 NM_001281494.2:c.1796G>A