Allele Registry

Canonical Allele Identifier: PA160901

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000121578

RCV000130273

RCV000409146

RCV000515340

RCV000588001

RCV001083152

RCV001356010

ClinVar Variation:

134851

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly355Ser	CA007937 NM_000179.3:c.1063G>A