Allele Registry

Canonical Allele Identifier: PA658680154

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000551898

RCV000776879

RCV003153678

RCV003226937

ClinVar Variation:

455296

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg128Cys	CA346737052 NM_000179.3:c.382C>T