Allele Registry

Canonical Allele Identifier: PA916011048

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000219210

RCV000697068

RCV001705217

RCV001942687

RCV003997941

RCV004040314

ClinVar Variation:

232033

1365556

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg62Ser	CA10578027 NM_001281492.2:c.184C>A CA2573134718 NM_001281492.2:c.183_184delinsAA