Allele Registry

Canonical Allele Identifier: PA2826627492

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000132477

RCV000202234

RCV000226221

RCV000656896

RCV001249963

RCV003333737

RCV003467198

ClinVar Variation:

142970

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Lys724del	CA010414 NM_001281492.2:c.2171_2173del