Allele Registry

Canonical Allele Identifier: PA169917

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000132477

RCV000202234

RCV000226221

RCV000656896

RCV001249963

RCV003333737

RCV003467198

ClinVar Variation:

142970

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Lys854del	CA010414 NM_000179.3:c.2561_2563del