Allele Registry

Canonical Allele Identifier: PA2826625976

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000168089

RCV000578381

RCV000657123

RCV001011904

ClinVar Variation:

188181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ala370Thr	CA008716 NM_001281492.2:c.1108G>A