Allele Registry

Canonical Allele Identifier: PA294429

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000131704

RCV000212633

RCV000557767

RCV000663288

RCV003467182

RCV003998115

ClinVar Variation:

142525

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro233Arg	CA016269 NM_000179.3:c.698C>G