Allele Registry

Canonical Allele Identifier: PA2826625104

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000583660

RCV000806695

RCV002466543

ClinVar Variation:

491994

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro163Ser	CA073534 NM_001281492.2:c.487C>T