Allele Registry

Canonical Allele Identifier: PA916011205

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000570481

RCV000758675

RCV001327550

ClinVar Variation:

487033

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Thr880Ile	CA069975 NM_001281492.2:c.2639C>T