Allele Registry

Canonical Allele Identifier: PA2826626983

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000132542

RCV002228511

RCV003998152

ClinVar Variation:

143023

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Tyr600Cys	CA009841 NM_001281492.2:c.1799A>G