Allele Registry

Canonical Allele Identifier: PA2826637056

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000409973

RCV000491707

RCV000524151

RCV000759857

RCV001290595

RCV003466945

RCV003997084

ClinVar Variation:

89333

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Lys712del	CA069980 NM_001281494.2:c.2134_2136del