Allele Registry

Canonical Allele Identifier: PA2826626828

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000822642

RCV001186406

RCV003450940

ClinVar Variation:

89248

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Cys564Arg	CA009656 NM_001281492.2:c.1690T>C