Allele Registry

Canonical Allele Identifier: PA2826627195

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160680

RCV000491573

RCV000659892

RCV001850271

ClinVar Variation:

182635

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro651Thr	CA010074 NM_001281492.2:c.1951C>A