Allele Registry

Canonical Allele Identifier: PA916011342

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491375

RCV000623149

RCV002051855

RCV002230108

RCV002272245

RCV004001829

ClinVar Variation:

410436

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Leu933Arg	CA16610953 NM_001281492.2:c.2798T>G