Allele Registry

Canonical Allele Identifier: PA2826625528

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000552028

RCV000570684

RCV000758608

RCV000985821

RCV002267855

ClinVar Variation:

127555

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Asp260Asn	CA008202 NM_001281492.2:c.778G>A