Allele Registry

Canonical Allele Identifier: PA658681032

Gene: MSH6 HGNC NCBI

ClinVar Allele:

451573

ClinVar RCV:

RCV000526734

RCV000567854

RCV004003680

ClinVar Variation:

455210

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Val867Ile	CA069233 NM_000179.3:c.2599G>A