Allele Registry

Canonical Allele Identifier: PA2826625257

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160712

RCV000214500

RCV000499861

RCV000818095

ClinVar Variation:

182657

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Thr197Ala	CA016717 NM_001281492.2:c.589A>G