Allele Registry

Canonical Allele Identifier: PA2826633343

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001971716

RCV002458921

ClinVar Variation:

1477689

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Glu891Ala	CA346760508 NM_001281493.2:c.2672A>C