Allele Registry

Canonical Allele Identifier: PA2826627809

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218606

RCV000486781

RCV000629928

RCV000805703

RCV003166251

RCV003468985

RCV004001679

ClinVar Variation:

229859

650537

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Thr794Ser	CA069606 NM_001281492.2:c.2380A>T CA346755462 NM_001281492.2:c.2381C>G