Allele Registry

Canonical Allele Identifier: PA658680204

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000570685

RCV001070096

RCV001844201

RCV004001062

ClinVar Variation:

483842

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg178Leu	CA346738710 NM_000179.3:c.533G>T