Allele Registry

Canonical Allele Identifier: PA287272

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115382

RCV000230963

RCV000235184

RCV000409045

RCV001192457

RCV003460812

RCV003758429

ClinVar Variation:

127563

2840176

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe582Leu	CA009115 NM_000179.3:c.1746T>G CA346748887 NM_000179.3:c.1744T>C CA346748902 NM_000179.3:c.1746T>A