Allele Registry

Canonical Allele Identifier: PA2826628622

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002455106

ClinVar Variation:

1732927

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser1065Ile	CA346760522 NM_001281492.2:c.3194G>T