Allele Registry

Canonical Allele Identifier: PA891846111

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000687058

ClinVar Variation:

567078

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Cys496Arg	CA346746069 NM_000179.3:c.1486T>C