Allele Registry

Canonical Allele Identifier: PA357674

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000206259

RCV002460058

RCV003462380

ClinVar Variation:

220489

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu381Lys	CA067195 NM_000179.3:c.1141G>A