Allele Registry

Canonical Allele Identifier: PA645382188

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000231716

RCV000483224

RCV000490886

RCV000986722

RCV003998718

ClinVar Variation:

237158

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Asn827Asp	CA10582063 NM_000179.3:c.2479A>G