Allele Registry

Canonical Allele Identifier: PA2826625961

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003078528

ClinVar Variation:

2161350

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Cys366Gly	CA346746070 NM_001281492.2:c.1096T>G