Allele Registry

Canonical Allele Identifier: PA2826631452

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129031

RCV000195792

RCV000657020

RCV000662484

RCV001002443

RCV003460882

RCV003997472

ClinVar Variation:

140836

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Arg459Gly	CA009950 NM_001281493.2:c.1375A>G