Allele Registry

Canonical Allele Identifier: PA2826625950

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001757554

ClinVar Variation:

1316107

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu363Asp	CA346746022 NM_001281492.2:c.1089G>C CA346746024 NM_001281492.2:c.1089G>T