Allele Registry

Canonical Allele Identifier: PA645379105

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000473462

RCV000568053

RCV000985853

RCV001821283

RCV004001830

ClinVar Variation:

410443

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu290Pro	CA073528 NM_000179.3:c.869T>C