Allele Registry

Canonical Allele Identifier: PA2826625123

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000165781

RCV000168235

RCV000588989

RCV000758602

RCV003320582

RCV003468757

ClinVar Variation:

186227

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg168Gln	CA016611 NM_001281492.2:c.503G>A