Allele Registry

Canonical Allele Identifier: PA2826626330

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115382

RCV000230963

RCV000235184

RCV000409045

RCV001192457

RCV003460812

RCV003758429

ClinVar Variation:

127563

2840176

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Phe452Leu	CA009115 NM_001281492.2:c.1356T>G CA346748887 NM_001281492.2:c.1354T>C CA346748902 NM_001281492.2:c.1356T>A