Allele Registry

Canonical Allele Identifier: PA191906

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000164843

RCV000485038

RCV000559935

RCV000659897

RCV003235031

RCV003460692

ClinVar Variation:

89461

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg1263Cys	CA014275 NM_000179.3:c.3787C>T