Allele Registry

Canonical Allele Identifier: PA2826624902

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000535308

RCV000571023

RCV004003702

ClinVar Variation:

455342

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ile115Val	CA346740050 NM_001281492.2:c.343A>G