Allele Registry

Canonical Allele Identifier: PA658680622

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000560586

RCV000567174

RCV000680207

RCV004003662

ClinVar Variation:

455141

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Cys496Tyr	CA067747 NM_000179.3:c.1487G>A