Allele Registry

Canonical Allele Identifier: PA2826626284

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001012805

ClinVar Variation:

819882

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly441Ser	CA346748571 NM_001281492.2:c.1321G>A