Allele Registry

Canonical Allele Identifier: PA645382191

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000217167

RCV000461932

RCV000985833

RCV002247652

RCV003462469

RCV003997908

ClinVar Variation:

231561

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser834Asn	CA069123 NM_000179.3:c.2501G>A