Allele Registry

Canonical Allele Identifier: PA2826626280

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002398931

ClinVar Variation:

1778592

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly441Ala	CA346748588 NM_001281492.2:c.1322G>C