Allele Registry

Canonical Allele Identifier: PA2826636266

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000231716

RCV000483224

RCV000490886

RCV000986722

RCV003998718

ClinVar Variation:

237158

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Asn525Asp	CA10582063 NM_001281494.2:c.1573A>G