Allele Registry

Canonical Allele Identifier: PA645382765

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218606

RCV000486781

RCV000629928

RCV000805703

RCV003166251

RCV003468985

RCV004001679

ClinVar Variation:

229859

650537

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr924Ser	CA069606 NM_000179.3:c.2770A>T CA346755462 NM_000179.3:c.2771C>G